Canonical Allele Identifier: CA2031042714
Gene:

Linked Data

dbSNP Id: rs1947024213

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40373567G>A , CM000674.2:g.40373567G>A GRCh38
NC_000012.11:g.40767369G>A , CM000674.1:g.40767369G>A GRCh37
NC_000012.10:g.39053636G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_944868.1:n.485-18740C>T
XR_944869.1:n.485-1515C>T
XR_001749087.1:n.380-1515C>T
XR_001749088.1:n.347-1515C>T
XR_944868.2:n.485-18740C>T
XR_944869.2:n.485-1515C>T