HGVS | Genome Assembly |
---|---|
NC_000013.11:g.20189410G>T , CM000675.2:g.20189410G>T | GRCh38 |
NC_000013.10:g.20763549G>T , CM000675.1:g.20763549G>T | GRCh37 |
NC_000013.9:g.19661549G>T | NCBI36 |
NG_008358.1:g.8566C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000382844.2:c.172C>A | ENSP00000372295.1:p.Pro58Thr | |
ENST00000382848.5:c.172C>A MANE Select | ENSP00000372299.4:p.Pro58Thr | |
ENST00000382844.1:c.172C>A | ENSP00000372295.1:p.Pro58Thr | |
ENST00000382848.4:c.172C>A | ENSP00000372299.4:p.Pro58Thr | |
NM_004004.5:c.172C>A | NP_003995.2:p.Pro58Thr | |
XM_011535049.1:c.172C>A | XP_011533351.1:p.Pro58Thr | |
XM_011535049.2:c.172C>A | XP_011533351.1:p.Pro58Thr | |
NM_004004.6:c.172C>A MANE Select | NP_003995.2:p.Pro58Thr |