Canonical Allele Identifier: CA11954982
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177086459A>G , CM000667.2:g.177086459A>G GRCh38
NC_000005.9:g.176513460A>G , CM000667.1:g.176513460A>G GRCh37
NC_000005.8:g.176446066A>G NCBI36
NG_012067.1:g.4540A>G

Transcript Alleles

HGVS Amino-acid Change
XR_941273.1:n.321A>G