Canonical Allele Identifier: CA1149396958
Gene:

Linked Data

dbSNP Id: rs1659182323

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2036480C>T , CM000663.2:g.2036480C>T GRCh38
NC_000001.10:g.1967919C>T , CM000663.1:g.1967919C>T GRCh37
NC_000001.9:g.1957779C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_946823.1:n.728G>A
XR_001737845.2:n.731G>A
XR_946823.3:n.731G>A