Canonical Allele Identifier: CA1439212904
Gene:

Linked Data

dbSNP Id: rs1711590310

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.12578270G>A , CM000666.2:g.12578270G>A GRCh38
NC_000004.11:g.12579894G>A , CM000666.1:g.12579894G>A GRCh37
NC_000004.10:g.12188992G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_925406.1:n.106+31072C>T
XR_001741374.1:n.254+44385C>T
XR_925406.3:n.140+31072C>T