Canonical Allele Identifier: CA604367412
Gene:

Linked Data

dbSNP Id: rs1362027277

Genomic Alleles

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

Transcript Alleles

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