Canonical Allele Identifier: CA1149397023
Gene:

Linked Data

dbSNP Id: rs1659183998

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2036563C>T , CM000663.2:g.2036563C>T GRCh38
NC_000001.10:g.1968002C>T , CM000663.1:g.1968002C>T GRCh37
NC_000001.9:g.1957862C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_946823.1:n.645G>A
XR_001737845.2:n.648G>A
XR_946823.3:n.648G>A