Canonical Allele Identifier: CA1439212967
Gene:

Linked Data

dbSNP Id: rs1577128570

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.12578339C>A , CM000666.2:g.12578339C>A GRCh38
NC_000004.11:g.12579963C>A , CM000666.1:g.12579963C>A GRCh37
NC_000004.10:g.12189061C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_925406.1:n.106+31003G>T
XR_001741374.1:n.254+44316G>T
XR_925406.3:n.140+31003G>T