Canonical Allele Identifier: CA2651782802
Gene: ADRA1D HGNC NCBI

Linked Data

gnomAD v4: 20-4221406-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.4221406T>C , CM000682.2:g.4221406T>C GRCh38
NC_000020.10:g.4202053T>C , CM000682.1:g.4202053T>C GRCh37
NC_000020.9:g.4150053T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000379453.6:c.*117A>G MANE Select ENSP00000368766.4:n.*117A>G
ENST00000379453.5:c.*117A>G ENSP00000368766.4:n.*117A>G
NM_000678.3:c.*117A>G NP_000669.1:n.*117A>G
NM_000678.4:c.*117A>G MANE Select NP_000669.1:n.*117A>G