Canonical Allele Identifier: CA1284431788
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122369181C= , CM000664.2:g.122369181C= GRCh38
NC_000002.11:g.123126757C= , CM000664.1:g.123126757C= GRCh37
NC_000002.10:g.122843227C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923278.1:n.556-23782C=
XR_001739684.1:n.556-23782C=