Canonical Allele Identifier: CA2346946176
Gene: ADRA1D HGNC NCBI

Linked Data

dbSNP Id: rs1981052872
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.4234880A>T , CM000682.2:g.4234880A>T GRCh38
NC_000020.10:g.4215527A>T , CM000682.1:g.4215527A>T GRCh37
NC_000020.9:g.4163527A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000379453.6:c.1112-12750T>A MANE Select ENSP00000368766.4:n.1112-12750T>A
ENST00000379453.5:c.1112-12750T>A ENSP00000368766.4:n.1112-12750T>A
NM_000678.3:c.1112-12750T>A NP_000669.1:n.1112-12750T>A
NM_000678.4:c.1112-12750T>A MANE Select NP_000669.1:n.1112-12750T>A
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