Canonical Allele Identifier: CA1438714408
Gene:

Linked Data

dbSNP Id: rs7671189

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.11673037T>A , CM000666.2:g.11673037T>A GRCh38
NC_000004.11:g.11674661T>A , CM000666.1:g.11674661T>A GRCh37
NC_000004.10:g.11283759T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001741361.1:n.1027-90422T>A