Canonical Allele Identifier: CA50327961
Gene:

Linked Data

dbSNP Id: rs945804743

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.74711969T>C , CM000664.2:g.74711969T>C GRCh38
NC_000002.11:g.74939096T>C , CM000664.1:g.74939096T>C GRCh37
NC_000002.10:g.74792604T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_427047.4:n.282T>C