HGVS | Genome Assembly |
---|---|
NC_000023.11:g.18507090T= , CM000685.2:g.18507090T= | GRCh38 |
NC_000023.10:g.18525210T= , CM000685.1:g.18525210T= | GRCh37 |
NC_000023.9:g.18435131T= | NCBI36 |
NG_008475.1:g.86486T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000623535.2:c.-7T= MANE Select | ENSP00000485244.1:n.-7T= | |
ENST00000635828.1:c.-7T= | ENSP00000490170.1:n.-7T= | |
ENST00000637881.1:c.-7T= | ENSP00000489879.1:n.-7T= | |
ENST00000674046.1:c.-7T= | ENSP00000501174.1:n.-7T= | |
ENST00000379989.6:c.-7T= | ENSP00000369325.3:n.-7T= | |
ENST00000379996.7:c.-7T= | ENSP00000369332.3:n.-7T= | |
ENST00000463994.4:c.-7T= | ENSP00000485184.1:n.-7T= | |
ENST00000623364.3:c.-7T= | ENSP00000485581.1:n.-7T= | |
ENST00000624700.3:c.-7T= | ENSP00000485359.1:n.-7T= | |
ENST00000624953.1:c.-7T= | ENSP00000485625.1:n.-7T= | |
NM_001037343.1:c.-7T= | NP_001032420.1:n.-7T= | |
NM_003159.2:c.-7T= | NP_003150.1:n.-7T= | |
XM_011545569.1:c.-7T= | XP_011543871.1:n.-7T= | |
XM_011545570.1:c.-93T= | XP_011543872.1:n.-93T= | |
XR_950484.1:n.246T= | ||
NM_001323289.1:c.-7T= | NP_001310218.1:n.-7T= | |
NM_001323289.2:c.-7T= MANE Select | NP_001310218.1:n.-7T= | |
NM_001037343.2:c.-7T= | NP_001032420.1:n.-7T= | |
NM_003159.3:c.-7T= | NP_003150.1:n.-7T= |