Canonical Allele Identifier: CA1283487516
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.120332095G= , CM000664.2:g.120332095G= GRCh38
NC_000002.11:g.121089671G= , CM000664.1:g.121089671G= GRCh37
NC_000002.10:g.120806141G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011512307.1:n.141+3289G= XP_011510609.1:p.=