Canonical Allele Identifier: CA1096188021
Gene:

Linked Data

dbSNP Id: rs1778854577

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155812341G>A , CM000668.2:g.155812341G>A GRCh38
NC_000006.11:g.156133475G>A , CM000668.1:g.156133475G>A GRCh37
NC_000006.10:g.156175167G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943142.1:n.79+18922G>A
XR_943146.1:n.645-302C>T
XR_001744423.1:n.699-302C>T
XR_001744424.1:n.79+18922G>A