Canonical Allele Identifier: CA1674885505
Gene:

Linked Data

dbSNP Id: rs1778853495

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155812266C>G , CM000668.2:g.155812266C>G GRCh38
NC_000006.11:g.156133400C>G , CM000668.1:g.156133400C>G GRCh37
NC_000006.10:g.156175092C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943142.1:n.79+18847C>G
XR_943146.1:n.645-227G>C
XR_001744423.1:n.699-227G>C
XR_001744424.1:n.79+18847C>G