Canonical Allele Identifier: CA29256304
Gene:

Linked Data

dbSNP Id: rs12061304

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.110695063A>G , CM000663.2:g.110695063A>G GRCh38
NC_000001.10:g.111237685A>G , CM000663.1:g.111237685A>G GRCh37
NC_000001.9:g.111039208A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001738182.1:n.649+8609A>G
XR_001738183.1:n.647+8609A>G
XR_001738184.1:n.653+8609A>G
XR_001738185.1:n.3278A>G
XR_001738186.1:n.652+8609A>G
XR_001738187.1:n.650+8609A>G