Canonical Allele Identifier: CA11137970
Gene:

Identifiers and link-outs to other resources

dbSNP Id: rs13387042

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.217041109A>G , CM000664.2:g.217041109A>G GRCh38
NC_000002.11:g.217905832A>G , CM000664.1:g.217905832A>G GRCh37
NC_000002.10:g.217614077A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923881.1:n.299+47091A>G
XR_923883.1:n.294+47091A>G
XR_923885.1:n.862+47091A>G
XR_923886.1:n.359-14082A>G
XR_923887.1:n.300-14082A>G
XR_001739169.1:n.11844+47091A>G
XR_001739170.2:n.8480+47091A>G
XR_001739171.2:n.8347+47091A>G
XR_923878.2:n.7422A>G