Canonical Allele Identifier: CA14837625
Gene: ADRA1D HGNC NCBI

Linked Data

dbSNP Id: rs1556832

Genomic Alleles

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

Transcript Alleles

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