Canonical Allele Identifier: CA311056398
Gene: ADRA1D HGNC NCBI

Linked Data

dbSNP Id: rs543084255
gnomAD v3: 20-4234733-G-C
gnomAD v4: 20-4234733-G-C
MyVariant Identifiers: chr20:g.4215380G>C (hg19) chr20:g.4234733G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.4234733G>C , CM000682.2:g.4234733G>C GRCh38
NC_000020.10:g.4215380G>C , CM000682.1:g.4215380G>C GRCh37
NC_000020.9:g.4163380G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000379453.6:c.1112-12603C>G MANE Select ENSP00000368766.4:n.1112-12603C>G
ENST00000379453.5:c.1112-12603C>G ENSP00000368766.4:n.1112-12603C>G
NM_000678.3:c.1112-12603C>G NP_000669.1:n.1112-12603C>G
NM_000678.4:c.1112-12603C>G MANE Select NP_000669.1:n.1112-12603C>G
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