Canonical Allele Identifier: CA2753840209
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.200033334C>G , CM000664.2:g.200033334C>G GRCh38
NC_000002.11:g.200898057C>G , CM000664.1:g.200898057C>G GRCh37
NC_000002.10:g.200606302C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923778.1:n.178-22438G>C