Canonical Allele Identifier: CA311056517

Gene: ADRA1D

Linked Data

• dbSNP Id: rs1007753829
• MyVariant Identifiers: chr20:g.4215475C>T (hg19) ; chr20:g.4234828C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.4234828C>T , CM000682.2:g.4234828C>T	GRCh38
NC_000020.10:g.4215475C>T , CM000682.1:g.4215475C>T	GRCh37
NC_000020.9:g.4163475C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000379453.6:c.1112-12698G>A MANE Select	ENSP00000368766.4:n.1112-12698G>A
ENST00000379453.5:c.1112-12698G>A	ENSP00000368766.4:n.1112-12698G>A
NM_000678.3:c.1112-12698G>A	NP_000669.1:n.1112-12698G>A
NM_000678.4:c.1112-12698G>A MANE Select	NP_000669.1:n.1112-12698G>A