Canonical Allele Identifier: CA2031042669
Gene:

Linked Data

dbSNP Id: rs1592362571

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40373534T>C , CM000674.2:g.40373534T>C GRCh38
NC_000012.11:g.40767336T>C , CM000674.1:g.40767336T>C GRCh37
NC_000012.10:g.39053603T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_944868.1:n.485-18707A>G
XR_944869.1:n.485-1482A>G
XR_001749087.1:n.380-1482A>G
XR_001749088.1:n.347-1482A>G
XR_944868.2:n.485-18707A>G
XR_944869.2:n.485-1482A>G