Canonical Allele Identifier: CA311056369
Gene: ADRA1D HGNC NCBI

Linked Data

dbSNP Id: rs1048546873
gnomAD v2: 20-4215376-T-C
gnomAD v3: 20-4234729-T-C
gnomAD v4: 20-4234729-T-C
MyVariant Identifiers: chr20:g.4215376T>C (hg19) chr20:g.4234729T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.4234729T>C , CM000682.2:g.4234729T>C GRCh38
NC_000020.10:g.4215376T>C , CM000682.1:g.4215376T>C GRCh37
NC_000020.9:g.4163376T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000379453.6:c.1112-12599A>G MANE Select ENSP00000368766.4:n.1112-12599A>G
ENST00000379453.5:c.1112-12599A>G ENSP00000368766.4:n.1112-12599A>G
NM_000678.3:c.1112-12599A>G NP_000669.1:n.1112-12599A>G
NM_000678.4:c.1112-12599A>G MANE Select NP_000669.1:n.1112-12599A>G
Search 100 bp 5'
Search 100 bp 3'