Canonical Allele Identifier: CA311056355
Gene: ADRA1D HGNC NCBI

Linked Data

dbSNP Id: rs921716654
gnomAD v3: 20-4234720-G-A
gnomAD v4: 20-4234720-G-A
MyVariant Identifiers: chr20:g.4215367G>A (hg19) chr20:g.4234720G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.4234720G>A , CM000682.2:g.4234720G>A GRCh38
NC_000020.10:g.4215367G>A , CM000682.1:g.4215367G>A GRCh37
NC_000020.9:g.4163367G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000379453.6:c.1112-12590C>T MANE Select ENSP00000368766.4:n.1112-12590C>T
ENST00000379453.5:c.1112-12590C>T ENSP00000368766.4:n.1112-12590C>T
NM_000678.3:c.1112-12590C>T NP_000669.1:n.1112-12590C>T
NM_000678.4:c.1112-12590C>T MANE Select NP_000669.1:n.1112-12590C>T
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