Canonical Allele Identifier: CA1387871354
Community Standard Title: NC_000003.12:g.99547493C=
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.99547493C= , CM000665.2:g.99547493C= GRCh38
NC_000003.11:g.99266337C= , CM000665.1:g.99266337C= GRCh37
NC_000003.10:g.100749027C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001740463.1:n.96+42114G=
XR_001740466.2:n.475G=
XR_924268.2:n.475G=