Canonical Allele Identifier: CA1674885489
Gene:

Linked Data

dbSNP Id: rs1583057045

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155812247T>G , CM000668.2:g.155812247T>G GRCh38
NC_000006.11:g.156133381T>G , CM000668.1:g.156133381T>G GRCh37
NC_000006.10:g.156175073T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943142.1:n.79+18828T>G
XR_943146.1:n.645-208A>C
XR_001744423.1:n.699-208A>C
XR_001744424.1:n.79+18828T>G