Canonical Allele Identifier: CA311056637
Gene: ADRA1D HGNC NCBI

Linked Data

dbSNP Id: rs958845138
MyVariant Identifiers: chr20:g.4215593A>G (hg19) chr20:g.4234946A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.4234946A>G , CM000682.2:g.4234946A>G GRCh38
NC_000020.10:g.4215593A>G , CM000682.1:g.4215593A>G GRCh37
NC_000020.9:g.4163593A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000379453.6:c.1112-12816T>C MANE Select ENSP00000368766.4:n.1112-12816T>C
ENST00000379453.5:c.1112-12816T>C ENSP00000368766.4:n.1112-12816T>C
NM_000678.3:c.1112-12816T>C NP_000669.1:n.1112-12816T>C
NM_000678.4:c.1112-12816T>C MANE Select NP_000669.1:n.1112-12816T>C
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