Canonical Allele Identifier: CA1674885546
Gene:

Linked Data

dbSNP Id: rs1562310268

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155812314A>G , CM000668.2:g.155812314A>G GRCh38
NC_000006.11:g.156133448A>G , CM000668.1:g.156133448A>G GRCh37
NC_000006.10:g.156175140A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943142.1:n.79+18895A>G
XR_943146.1:n.645-275T>C
XR_001744423.1:n.699-275T>C
XR_001744424.1:n.79+18895A>G