HGVS | Genome Assembly |
---|---|
NC_000014.9:g.23423485_23423486insGA , CM000676.2:g.23423485_23423486insGA | GRCh38 |
NC_000014.8:g.23892694_23892695insGA , CM000676.1:g.23892694_23892695insGA | GRCh37 |
NC_000014.7:g.22962534_22962535insGA | NCBI36 |
NG_007884.1:g.17177_17178insCT , LRG_384:g.17177_17178insCT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000355349.4:c.3099+62_3099+63insCT MANE Select | ENSP00000347507.3:n.3099+62_3099+63insCT | |
ENST00000355349.3:c.3099+62_3099+63insCT | ENSP00000347507.3:n.3099+62_3099+63insCT | |
NM_000257.3:c.3099+62_3099+63insCT | NP_000248.2:n.3099+62_3099+63insCT | |
XR_245686.3:n.3205+62_3205+63insCT | ||
XM_017021340.1:c.3099+62_3099+63insCT | XP_016876829.1:n.3099+62_3099+63insCT | |
NM_000257.4:c.3099+62_3099+63insCT MANE Select | NP_000248.2:n.3099+62_3099+63insCT |