Canonical Allele Identifier: CA1282457844
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.118083157G= , CM000664.2:g.118083157G= GRCh38
NC_000002.11:g.118840733G= , CM000664.1:g.118840733G= GRCh37
NC_000002.10:g.118557203G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011512305.1:c.696+4903C= XP_011510607.1:n.696+4903C=
XR_001739662.2:n.138+5094C=