Canonical Allele Identifier: CA65985376
Gene:

Identifiers and link-outs to other resources

dbSNP Id: rs10932688

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.216998758C>G , CM000664.2:g.216998758C>G GRCh38
NC_000002.11:g.217863481C>G , CM000664.1:g.217863481C>G GRCh37
NC_000002.10:g.217571726C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923881.1:n.299+4740C>G
XR_923883.1:n.294+4740C>G
XR_923885.1:n.862+4740C>G
XR_923886.1:n.300-2289C>G
XR_923887.1:n.299+4740C>G
XR_001739169.1:n.11844+4740C>G
XR_001739170.2:n.8480+4740C>G
XR_001739171.2:n.8347+4740C>G