Canonical Allele Identifier: CA1439212733
Gene:

Linked Data

dbSNP Id: rs1711582014

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.12578112G>T , CM000666.2:g.12578112G>T GRCh38
NC_000004.11:g.12579736G>T , CM000666.1:g.12579736G>T GRCh37
NC_000004.10:g.12188834G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_925406.1:n.106+31230C>A
XR_001741374.1:n.254+44543C>A
XR_925406.3:n.140+31230C>A