Canonical Allele Identifier: CA634198534
Gene: ADRA1D HGNC NCBI

Linked Data

dbSNP Id: rs1220864601
gnomAD v2: 20-4215556-C-T
gnomAD v3: 20-4234909-C-T
gnomAD v4: 20-4234909-C-T
MyVariant Identifiers: chr20:g.4215556C>T (hg19) chr20:g.4234909C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.4234909C>T , CM000682.2:g.4234909C>T GRCh38
NC_000020.10:g.4215556C>T , CM000682.1:g.4215556C>T GRCh37
NC_000020.9:g.4163556C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000379453.6:c.1112-12779G>A MANE Select ENSP00000368766.4:n.1112-12779G>A
ENST00000379453.5:c.1112-12779G>A ENSP00000368766.4:n.1112-12779G>A
NM_000678.3:c.1112-12779G>A NP_000669.1:n.1112-12779G>A
NM_000678.4:c.1112-12779G>A MANE Select NP_000669.1:n.1112-12779G>A
Search 100 bp 5'
Search 100 bp 3'