Canonical Allele Identifier: CA1010607893
Gene:

Linked Data

dbSNP Id: rs1675445933

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193121717A>G , CM000663.2:g.193121717A>G GRCh38
NC_000001.10:g.193090847A>G , CM000663.1:g.193090847A>G GRCh37
NC_000001.9:g.191357470A>G NCBI36
NG_012691.1:g.4760A>G , LRG_507:g.4760A>G

Transcript Alleles

HGVS Amino-acid Change
XR_001738350.1:n.1940T>C