Canonical Allele Identifier: CA2736264502
Gene: ADRA1D HGNC NCBI

Linked Data

dbSNP Id: rs2122666965
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.4235003T>C , CM000682.2:g.4235003T>C GRCh38
NC_000020.10:g.4215650T>C , CM000682.1:g.4215650T>C GRCh37
NC_000020.9:g.4163650T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000379453.6:c.1111+12844A>G MANE Select ENSP00000368766.4:n.1111+12844A>G
ENST00000379453.5:c.1111+12844A>G ENSP00000368766.4:n.1111+12844A>G
NM_000678.3:c.1111+12844A>G NP_000669.1:n.1111+12844A>G
NM_000678.4:c.1111+12844A>G MANE Select NP_000669.1:n.1111+12844A>G
Search 100 bp 5'
Search 100 bp 3'