Canonical Allele Identifier: CA586167841
Gene: DMRT1 HGNC NCBI

Linked Data

dbSNP Id: rs1013014003
gnomAD v2: 9-841801-G-A
gnomAD v4: 9-841801-G-A
MyVariant Identifiers: chr9:g.841801_841802delinsAA (hg19) chr9:g.841801_841802delinsAA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.841801G>A , CM000671.2:g.841801G>A GRCh38
NC_000009.11:g.841801G>A , CM000671.1:g.841801G>A GRCh37
NC_000009.10:g.831801G>A NCBI36
NG_009221.1:g.5112G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000382276.8:c.-38G>A MANE Select ENSP00000371711.3:n.-38G>A
ENST00000382276.7:c.-38G>A ENSP00000371711.3:n.-38G>A
ENST00000564322.1:n.112G>A
NM_021951.2:c.-38G>A NP_068770.2:n.-38G>A
XM_006716732.1:c.-38G>A XP_006716795.1:n.-38G>A
XM_017014375.1:c.-38G>A XP_016869864.1:n.-38G>A
NM_021951.3:c.-38G>A MANE Select NP_068770.2:n.-38G>A
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