Canonical Allele Identifier: CA946078298
Gene:

Linked Data

dbSNP Id: rs1944931943

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.29960956T>G , CM000674.2:g.29960956T>G GRCh38
NC_000012.11:g.30113889T>G , CM000674.1:g.30113889T>G GRCh37
NC_000012.10:g.30005156T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_931473.1:n.314-17916A>C
XR_931474.1:n.314-17916A>C
XR_931475.1:n.135-17916A>C
XR_001749060.1:n.314-17916A>C
XR_001749061.1:n.314-17916A>C