Canonical Allele Identifier: CA1284431900
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122369376C= , CM000664.2:g.122369376C= GRCh38
NC_000002.11:g.123126952C= , CM000664.1:g.123126952C= GRCh37
NC_000002.10:g.122843422C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923278.1:n.556-23587C=
XR_001739684.1:n.556-23587C=