Canonical Allele Identifier: CA16841709
Gene:

Linked Data

dbSNP Id: rs925694592

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2036525C>T , CM000663.2:g.2036525C>T GRCh38
NC_000001.10:g.1967964C>T , CM000663.1:g.1967964C>T GRCh37
NC_000001.9:g.1957824C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_946823.1:n.683G>A
XR_001737845.2:n.686G>A
XR_946823.3:n.686G>A