Canonical Allele Identifier: CA311056658

Gene: ADRA1D

Linked Data

• dbSNP Id: rs530331564
• gnomAD v2: 20-4215608-G-A
• gnomAD v3: 20-4234961-G-A
• gnomAD v4: 20-4234961-G-A
• MyVariant Identifiers: chr20:g.4215608G>A (hg19) ; chr20:g.4234961G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.4234961G>A , CM000682.2:g.4234961G>A	GRCh38
NC_000020.10:g.4215608G>A , CM000682.1:g.4215608G>A	GRCh37
NC_000020.9:g.4163608G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000379453.6:c.1112-12831C>T MANE Select	ENSP00000368766.4:n.1112-12831C>T
ENST00000379453.5:c.1112-12831C>T	ENSP00000368766.4:n.1112-12831C>T
NM_000678.3:c.1112-12831C>T	NP_000669.1:n.1112-12831C>T
NM_000678.4:c.1112-12831C>T MANE Select	NP_000669.1:n.1112-12831C>T