Canonical Allele Identifier: CA2025046520
Gene:

Linked Data

dbSNP Id: rs1944932189

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.29961012G>A , CM000674.2:g.29961012G>A GRCh38
NC_000012.11:g.30113945G>A , CM000674.1:g.30113945G>A GRCh37
NC_000012.10:g.30005212G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_931473.1:n.314-17972C>T
XR_931474.1:n.314-17972C>T
XR_931475.1:n.135-17972C>T
XR_001749060.1:n.314-17972C>T
XR_001749061.1:n.314-17972C>T