Canonical Allele Identifier: CA744516568

Gene: ADRA1D

Linked Data

• dbSNP Id: rs1556832
• MyVariant Identifiers: chr20:g.4215557C>G (hg19) ; chr20:g.4234910C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.4234910C>G , CM000682.2:g.4234910C>G	GRCh38
NC_000020.10:g.4215557C>G , CM000682.1:g.4215557C>G	GRCh37
NC_000020.9:g.4163557C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000379453.6:c.1112-12780G>C MANE Select	ENSP00000368766.4:n.1112-12780G>C
ENST00000379453.5:c.1112-12780G>C	ENSP00000368766.4:n.1112-12780G>C
NM_000678.3:c.1112-12780G>C	NP_000669.1:n.1112-12780G>C
NM_000678.4:c.1112-12780G>C MANE Select	NP_000669.1:n.1112-12780G>C