Canonical Allele Identifier: CA2031042737
Gene:

Linked Data

dbSNP Id: rs1947024379

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40373592C>G , CM000674.2:g.40373592C>G GRCh38
NC_000012.11:g.40767394C>G , CM000674.1:g.40767394C>G GRCh37
NC_000012.10:g.39053661C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_944868.1:n.485-18765G>C
XR_944869.1:n.485-1540G>C
XR_001749087.1:n.380-1540G>C
XR_001749088.1:n.347-1540G>C
XR_944868.2:n.485-18765G>C
XR_944869.2:n.485-1540G>C