Canonical Allele Identifier: CA2710750424
Gene:

Linked Data

dbSNP Id: rs973439562

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.11943349T>A , CM000668.2:g.11943349T>A GRCh38
NC_000006.11:g.11943582T>A , CM000668.1:g.11943582T>A GRCh37
NC_000006.10:g.12051568T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001743976.1:n.348-8186T>A