Canonical Allele Identifier: CA1439212961
Gene:

Linked Data

dbSNP Id: rs1711591277

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.12578332C>A , CM000666.2:g.12578332C>A GRCh38
NC_000004.11:g.12579956C>A , CM000666.1:g.12579956C>A GRCh37
NC_000004.10:g.12189054C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_925406.1:n.106+31010G>T
XR_001741374.1:n.254+44323G>T
XR_925406.3:n.140+31010G>T