Canonical Allele Identifier: CA821943367
Gene:

Linked Data

dbSNP Id: rs1183500822

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.163765693A>G , CM000668.2:g.163765693A>G GRCh38
NC_000006.11:g.164186725A>G , CM000668.1:g.164186725A>G GRCh37
NC_000006.10:g.164106715A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001744452.1:n.410+6264A>G
XR_001744454.1:n.369+6305A>G
XR_001744455.1:n.346+6328A>G