Canonical Allele Identifier: CA1041166111
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.200033291T>C , CM000664.2:g.200033291T>C GRCh38
NC_000002.11:g.200898014T>C , CM000664.1:g.200898014T>C GRCh37
NC_000002.10:g.200606259T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923778.1:n.178-22395A>G