Canonical Allele Identifier: CA2736264503
Gene: ADRA1D HGNC NCBI

Linked Data

dbSNP Id: rs2122666973

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.4235011G>A , CM000682.2:g.4235011G>A GRCh38
NC_000020.10:g.4215658G>A , CM000682.1:g.4215658G>A GRCh37
NC_000020.9:g.4163658G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000379453.6:c.1111+12836C>T MANE Select ENSP00000368766.4:n.1111+12836C>T
ENST00000379453.5:c.1111+12836C>T ENSP00000368766.4:n.1111+12836C>T
NM_000678.3:c.1111+12836C>T NP_000669.1:n.1111+12836C>T
NM_000678.4:c.1111+12836C>T MANE Select NP_000669.1:n.1111+12836C>T