Canonical Allele Identifier: CA1216113094
Gene:

Linked Data

dbSNP Id: rs1675446276

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193121730G>A , CM000663.2:g.193121730G>A GRCh38
NC_000001.10:g.193090860G>A , CM000663.1:g.193090860G>A GRCh37
NC_000001.9:g.191357483G>A NCBI36
NG_012691.1:g.4773G>A , LRG_507:g.4773G>A

Transcript Alleles

HGVS Amino-acid Change
XR_001738350.1:n.1927C>T