Canonical Allele Identifier: CA913365519
Gene:

Linked Data

dbSNP Id: rs1558275610

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193121748T>C , CM000663.2:g.193121748T>C GRCh38
NC_000001.10:g.193090878T>C , CM000663.1:g.193090878T>C GRCh37
NC_000001.9:g.191357501T>C NCBI36
NG_012691.1:g.4791T>C , LRG_507:g.4791T>C

Transcript Alleles

HGVS Amino-acid Change
XR_001738350.1:n.1909A>G