Canonical Allele Identifier: CA64382868
Gene:

Linked Data

dbSNP Id: rs894747476

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.200033111T>G , CM000664.2:g.200033111T>G GRCh38
NC_000002.11:g.200897834T>G , CM000664.1:g.200897834T>G GRCh37
NC_000002.10:g.200606079T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923778.1:n.178-22215A>C