Canonical Allele Identifier: CA39003138
Gene:

Linked Data

dbSNP Id: rs1028233715

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.224887101T>C , CM000663.2:g.224887101T>C GRCh38
NC_000001.10:g.225074803T>C , CM000663.1:g.225074803T>C GRCh37
NC_000001.9:g.223141426T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_949207.1:n.66-2320A>G
XR_949207.2:n.63-2320A>G