Canonical Allele Identifier: CA2346939758
Gene: ADRA1D HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.4221303A= , CM000682.2:g.4221303A= GRCh38
NC_000020.10:g.4201950A= , CM000682.1:g.4201950A= GRCh37
NC_000020.9:g.4149950A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000379453.6:c.*220T= MANE Select ENSP00000368766.4:n.*220T=
ENST00000379453.5:c.*220T= ENSP00000368766.4:n.*220T=
NM_000678.3:c.*220T= NP_000669.1:n.*220T=
NM_000678.4:c.*220T= MANE Select NP_000669.1:n.*220T=
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