Canonical Allele Identifier: CA200964111
Gene: DBH HGNC NCBI

Linked Data

dbSNP Id: rs745753766
gnomAD v2: 9-136509545-T-C
gnomAD v3: 9-133644423-T-C
gnomAD v4: 9-133644423-T-C
MyVariant Identifiers: chr9:g.136509545T>C (hg19) chr9:g.133644423T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133644423T>C , CM000671.2:g.133644423T>C GRCh38
NC_000009.11:g.136509545T>C , CM000671.1:g.136509545T>C GRCh37
NC_000009.10:g.135499366T>C NCBI36
NG_008645.1:g.13061T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000393056.8:c.1024+103T>C MANE Select ENSP00000376776.2:n.1024+103T>C
ENST00000393056.6:c.1024+103T>C ENSP00000376776.2:n.1024+103T>C
NM_000787.3:c.1024+103T>C NP_000778.3:n.1024+103T>C
NM_000787.4:c.1024+103T>C MANE Select NP_000778.3:n.1024+103T>C
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