Canonical Allele Identifier: CA2346939763
Gene: ADRA1D HGNC NCBI

Linked Data

dbSNP Id: rs1600843232

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.4221309G>A , CM000682.2:g.4221309G>A GRCh38
NC_000020.10:g.4201956G>A , CM000682.1:g.4201956G>A GRCh37
NC_000020.9:g.4149956G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000379453.6:c.*214C>T MANE Select ENSP00000368766.4:n.*214C>T
ENST00000379453.5:c.*214C>T ENSP00000368766.4:n.*214C>T
NM_000678.3:c.*214C>T NP_000669.1:n.*214C>T
NM_000678.4:c.*214C>T MANE Select NP_000669.1:n.*214C>T