Canonical Allele Identifier: CA1109769921
Gene:

Linked Data

dbSNP Id: rs1799898301
gnomAD v3: 8-2883014-T-G
gnomAD v4: 8-2883014-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.2883014T>G , CM000670.2:g.2883014T>G GRCh38
NC_000008.10:g.2740536T>G , CM000670.1:g.2740536T>G GRCh37
NC_000008.9:g.2727943T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_941367.1:n.212-42751T>G
NR_168441.1:n.1166+45250T>G
NR_168442.1:n.1331-33321T>G
NR_168443.1:n.1171+45250T>G
NR_168444.1:n.1166+45250T>G
NR_168445.1:n.1249+45167T>G