Canonical Allele Identifier: CA2346946228
Gene: ADRA1D HGNC NCBI

Linked Data

dbSNP Id: rs1981055565

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.4234977T>C , CM000682.2:g.4234977T>C GRCh38
NC_000020.10:g.4215624T>C , CM000682.1:g.4215624T>C GRCh37
NC_000020.9:g.4163624T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000379453.6:c.1112-12847A>G MANE Select ENSP00000368766.4:n.1112-12847A>G
ENST00000379453.5:c.1112-12847A>G ENSP00000368766.4:n.1112-12847A>G
NM_000678.3:c.1112-12847A>G NP_000669.1:n.1112-12847A>G
NM_000678.4:c.1112-12847A>G MANE Select NP_000669.1:n.1112-12847A>G