Canonical Allele Identifier: CA1224247021
Gene:

Linked Data

dbSNP Id: rs1691411332

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.224887113A>C , CM000663.2:g.224887113A>C GRCh38
NC_000001.10:g.225074815A>C , CM000663.1:g.225074815A>C GRCh37
NC_000001.9:g.223141438A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_949207.1:n.66-2332T>G
XR_949207.2:n.63-2332T>G