Canonical Allele Identifier: CA538890442
Gene:

Linked Data

dbSNP Id: rs1349867961

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.200033096A>G , CM000664.2:g.200033096A>G GRCh38
NC_000002.11:g.200897819A>G , CM000664.1:g.200897819A>G GRCh37
NC_000002.10:g.200606064A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923778.1:n.178-22200T>C