Canonical Allele Identifier: CA1758307093
Gene:

Linked Data

dbSNP Id: rs1799897883

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.2882988A>G , CM000670.2:g.2882988A>G GRCh38
NC_000008.10:g.2740510A>G , CM000670.1:g.2740510A>G GRCh37
NC_000008.9:g.2727917A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_941367.1:n.212-42777A>G
NR_168441.1:n.1166+45224A>G
NR_168442.1:n.1331-33347A>G
NR_168443.1:n.1171+45224A>G
NR_168444.1:n.1166+45224A>G
NR_168445.1:n.1249+45141A>G