Canonical Allele Identifier: CA4961397
Gene: DMRT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1280767
ClinVar RCV Id: RCV001688786
dbSNP Id: rs3739584
ExAC: 9:841825 C / T
gnomAD v2: 9-841825-C-T
gnomAD v3: 9-841825-C-T
gnomAD v4: 9-841825-C-T
MyVariant Identifiers: chr9:g.841825C>T (hg19) chr9:g.841825C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.841825C>T , CM000671.2:g.841825C>T GRCh38
NC_000009.11:g.841825C>T , CM000671.1:g.841825C>T GRCh37
NC_000009.10:g.831825C>T NCBI36
NG_009221.1:g.5136C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000382276.8:c.-14C>T MANE Select ENSP00000371711.3:n.-14C>T
ENST00000382276.7:c.-14C>T ENSP00000371711.3:n.-14C>T
ENST00000564322.1:n.136C>T
NM_021951.2:c.-14C>T NP_068770.2:n.-14C>T
XM_006716732.1:c.-14C>T XP_006716795.1:n.-14C>T
XM_017014375.1:c.-14C>T XP_016869864.1:n.-14C>T
NM_021951.3:c.-14C>T MANE Select NP_068770.2:n.-14C>T
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