Canonical Allele Identifier: CA1010607936
Gene:

Linked Data

dbSNP Id: rs1675447756

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193121782C>T , CM000663.2:g.193121782C>T GRCh38
NC_000001.10:g.193090912C>T , CM000663.1:g.193090912C>T GRCh37
NC_000001.9:g.191357535C>T NCBI36
NG_012691.1:g.4825C>T , LRG_507:g.4825C>T

Transcript Alleles

HGVS Amino-acid Change
XR_001738350.1:n.1875G>A