Canonical Allele Identifier: CA1094772219
Gene:

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.134773036G>T , CM000668.2:g.134773036G>T GRCh38
NC_000006.11:g.135094174G>T , CM000668.1:g.135094174G>T GRCh37
NC_000006.10:g.135135867G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943008.1:n.368+32702C>A
XR_943009.1:n.368+32702C>A
XR_001744363.1:n.414+32702C>A
XR_001744364.1:n.342+32702C>A