Canonical Allele Identifier: CA1094772251
Gene:

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.134773041T>C , CM000668.2:g.134773041T>C GRCh38
NC_000006.11:g.135094179T>C , CM000668.1:g.135094179T>C GRCh37
NC_000006.10:g.135135872T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943008.1:n.368+32697A>G
XR_943009.1:n.368+32697A>G
XR_001744363.1:n.414+32697A>G
XR_001744364.1:n.342+32697A>G