Canonical Allele Identifier: CA2025046512
Gene:

Linked Data

dbSNP Id: rs1362027277

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.29961002C>A , CM000674.2:g.29961002C>A GRCh38
NC_000012.11:g.30113935C>A , CM000674.1:g.30113935C>A GRCh37
NC_000012.10:g.30005202C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_931473.1:n.314-17962G>T
XR_931474.1:n.314-17962G>T
XR_931475.1:n.135-17962G>T
XR_001749060.1:n.314-17962G>T
XR_001749061.1:n.314-17962G>T