Canonical Allele Identifier: CA311056678
Gene: ADRA1D HGNC NCBI

Linked Data

dbSNP Id: rs991357300
MyVariant Identifiers: chr20:g.4215630C>G (hg19) chr20:g.4234983C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.4234983C>G , CM000682.2:g.4234983C>G GRCh38
NC_000020.10:g.4215630C>G , CM000682.1:g.4215630C>G GRCh37
NC_000020.9:g.4163630C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000379453.6:c.1112-12853G>C MANE Select ENSP00000368766.4:n.1112-12853G>C
ENST00000379453.5:c.1112-12853G>C ENSP00000368766.4:n.1112-12853G>C
NM_000678.3:c.1112-12853G>C NP_000669.1:n.1112-12853G>C
NM_000678.4:c.1112-12853G>C MANE Select NP_000669.1:n.1112-12853G>C
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