Canonical Allele Identifier: CA1758346754
Gene:

Linked Data

dbSNP Id: rs1800980795

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.2923360C>G , CM000670.2:g.2923360C>G GRCh38
NC_000008.10:g.2780882C>G , CM000670.1:g.2780882C>G GRCh37
NC_000008.9:g.2768289C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_941365.1:n.127+202G>C
XR_941367.1:n.212-2405C>G
XR_002956657.1:n.1002-2405C>G
XR_002956658.1:n.3030-2405C>G
NR_168441.1:n.1167-77645C>G
NR_168442.1:n.1698-2405C>G
NR_168443.1:n.1172-85208C>G
NR_168444.1:n.1167-66178C>G
NR_168445.1:n.1250-66178C>G