Canonical Allele Identifier: CA2346946178
Gene: ADRA1D HGNC NCBI

Linked Data

dbSNP Id: rs1981052943

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.4234891A>T , CM000682.2:g.4234891A>T GRCh38
NC_000020.10:g.4215538A>T , CM000682.1:g.4215538A>T GRCh37
NC_000020.9:g.4163538A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000379453.6:c.1112-12761T>A MANE Select ENSP00000368766.4:n.1112-12761T>A
ENST00000379453.5:c.1112-12761T>A ENSP00000368766.4:n.1112-12761T>A
NM_000678.3:c.1112-12761T>A NP_000669.1:n.1112-12761T>A
NM_000678.4:c.1112-12761T>A MANE Select NP_000669.1:n.1112-12761T>A