Canonical Allele Identifier: CA1882777234
Gene: DBH HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133644339_133644342delinsATCC , CM000671.2:g.133644339_133644342delinsATCC GRCh38
NC_000009.11:g.136509461_136509464delinsATCC , CM000671.1:g.136509461_136509464delinsATCC GRCh37
NC_000009.10:g.135499282_135499285delinsATCC NCBI36
NG_008645.1:g.12977_12980delinsATCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000393056.8:c.1024+19_1024+22delinsATCC MANE Select ENSP00000376776.2:n.1024+19_1024+22delinsATCC
ENST00000393056.6:c.1024+19_1024+22delinsATCC ENSP00000376776.2:n.1024+19_1024+22delinsATCC
NM_000787.3:c.1024+19_1024+22delinsATCC NP_000778.3:n.1024+19_1024+22delinsATCC
NM_000787.4:c.1024+19_1024+22delinsATCC MANE Select NP_000778.3:n.1024+19_1024+22delinsATCC
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