Canonical Allele Identifier: CA1096188023
Gene:

Linked Data

dbSNP Id: rs1778854663

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155812343A>G , CM000668.2:g.155812343A>G GRCh38
NC_000006.11:g.156133477A>G , CM000668.1:g.156133477A>G GRCh37
NC_000006.10:g.156175169A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943142.1:n.79+18924A>G
XR_943146.1:n.645-304T>C
XR_001744423.1:n.699-304T>C
XR_001744424.1:n.79+18924A>G