Canonical Allele Identifier: CA2971451846
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.120332181G>A , CM000664.2:g.120332181G>A GRCh38
NC_000002.11:g.121089757G>A , CM000664.1:g.121089757G>A GRCh37
NC_000002.10:g.120806227G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011512307.1:c.141+3375G>A XP_011510609.1:n.141+3375G>A