Canonical Allele Identifier: CA1282455950
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.118078449C= , CM000664.2:g.118078449C= GRCh38
NC_000002.11:g.118836025C= , CM000664.1:g.118836025C= GRCh37
NC_000002.10:g.118552495C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011512305.1:c.697-917G= XP_011510607.1:n.697-917G=
XR_001739662.2:n.138+9802G=