Canonical Allele Identifier: CA1237562184
Community Standard Title: NC_000002.12:g.21617221C=
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21617221C= , CM000664.2:g.21617221C= GRCh38
NC_000002.11:g.21840093C= , CM000664.1:g.21840093C= GRCh37
NC_000002.10:g.21693598C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001739327.1:n.2811-9311G=
XR_939810.1:n.2647-9311G=