Canonical Allele Identifier: CA604367416
Gene:

Linked Data

dbSNP Id: rs1313191977

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.29961065G>A , CM000674.2:g.29961065G>A GRCh38
NC_000012.11:g.30113998G>A , CM000674.1:g.30113998G>A GRCh37
NC_000012.10:g.30005265G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_931473.1:n.314-18025C>T
XR_931474.1:n.314-18025C>T
XR_931475.1:n.135-18025C>T
XR_001749060.1:n.314-18025C>T
XR_001749061.1:n.314-18025C>T