Canonical Allele Identifier: CA2649624384
Gene:

Linked Data

dbSNP Id: rs2103110923

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193121892G>T , CM000663.2:g.193121892G>T GRCh38
NC_000001.10:g.193091022G>T , CM000663.1:g.193091022G>T GRCh37
NC_000001.9:g.191357645G>T NCBI36
NG_012691.1:g.4935G>T , LRG_507:g.4935G>T

Transcript Alleles

HGVS Amino-acid Change
XR_001738350.1:n.1765C>A