Canonical Allele Identifier: CA16841754
Gene:

Linked Data

dbSNP Id: rs954650595

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2036567A>G , CM000663.2:g.2036567A>G GRCh38
NC_000001.10:g.1968006A>G , CM000663.1:g.1968006A>G GRCh37
NC_000001.9:g.1957866A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_946823.1:n.641T>C
XR_001737845.2:n.644T>C
XR_946823.3:n.644T>C