Canonical Allele Identifier: CA2649624235
Gene:

Linked Data

dbSNP Id: rs2103110647

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193121757G>A , CM000663.2:g.193121757G>A GRCh38
NC_000001.10:g.193090887G>A , CM000663.1:g.193090887G>A GRCh37
NC_000001.9:g.191357510G>A NCBI36
NG_012691.1:g.4800G>A , LRG_507:g.4800G>A

Transcript Alleles

HGVS Amino-acid Change
XR_001738350.1:n.1900C>T