Canonical Allele Identifier: CA634198283
Gene: ADRA1D HGNC NCBI

Linked Data

dbSNP Id: rs1413974712
gnomAD v2: 20-4215391-C-T
gnomAD v3: 20-4234744-C-T
gnomAD v4: 20-4234744-C-T
MyVariant Identifiers: chr20:g.4215391C>T (hg19) chr20:g.4234744C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.4234744C>T , CM000682.2:g.4234744C>T GRCh38
NC_000020.10:g.4215391C>T , CM000682.1:g.4215391C>T GRCh37
NC_000020.9:g.4163391C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000379453.6:c.1112-12614G>A MANE Select ENSP00000368766.4:n.1112-12614G>A
ENST00000379453.5:c.1112-12614G>A ENSP00000368766.4:n.1112-12614G>A
NM_000678.3:c.1112-12614G>A NP_000669.1:n.1112-12614G>A
NM_000678.4:c.1112-12614G>A MANE Select NP_000669.1:n.1112-12614G>A
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