Canonical Allele Identifier: CA2649624429
Gene:

Linked Data

dbSNP Id: rs2103110981

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193121930C>T , CM000663.2:g.193121930C>T GRCh38
NC_000001.10:g.193091060C>T , CM000663.1:g.193091060C>T GRCh37
NC_000001.9:g.191357683C>T NCBI36
NG_012691.1:g.4973C>T , LRG_507:g.4973C>T

Transcript Alleles

HGVS Amino-acid Change
XR_001738350.1:n.1727G>A