Canonical Allele Identifier: CA744516445
Gene: ADRA1D HGNC NCBI

Linked Data

dbSNP Id: rs1382942710
MyVariant Identifiers: chr20:g.4215371C>T (hg19) chr20:g.4234724C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.4234724C>T , CM000682.2:g.4234724C>T GRCh38
NC_000020.10:g.4215371C>T , CM000682.1:g.4215371C>T GRCh37
NC_000020.9:g.4163371C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000379453.6:c.1112-12594G>A MANE Select ENSP00000368766.4:n.1112-12594G>A
ENST00000379453.5:c.1112-12594G>A ENSP00000368766.4:n.1112-12594G>A
NM_000678.3:c.1112-12594G>A NP_000669.1:n.1112-12594G>A
NM_000678.4:c.1112-12594G>A MANE Select NP_000669.1:n.1112-12594G>A
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