Canonical Allele Identifier: CA2346946250
Gene: ADRA1D HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.4235040C= , CM000682.2:g.4235040C= GRCh38
NC_000020.10:g.4215687C= , CM000682.1:g.4215687C= GRCh37
NC_000020.9:g.4163687C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000379453.6:c.1111+12807G= MANE Select ENSP00000368766.4:n.1111+12807G=
ENST00000379453.5:c.1111+12807G= ENSP00000368766.4:n.1111+12807G=
NM_000678.3:c.1111+12807G= NP_000669.1:n.1111+12807G=
NM_000678.4:c.1111+12807G= MANE Select NP_000669.1:n.1111+12807G=
Search 100 bp 5'
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