Canonical Allele Identifier: CA145511533
Gene:

Linked Data

dbSNP Id: rs996031909

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.105805173G>A , CM000668.2:g.105805173G>A GRCh38
NC_000006.11:g.106253048G>A , CM000668.1:g.106253048G>A GRCh37
NC_000006.10:g.106359741G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_942835.1:n.510+24884C>T
XR_001744274.1:n.438+24884C>T
XR_001744275.1:n.337+24884C>T