Canonical Allele Identifier: CA586167846
Gene: DMRT1 HGNC NCBI

Linked Data

dbSNP Id: rs1409137775
gnomAD v2: 9-841822-C-T
gnomAD v4: 9-841822-C-T
MyVariant Identifiers: chr9:g.841822C>T (hg19) chr9:g.841822C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.841822C>T , CM000671.2:g.841822C>T GRCh38
NC_000009.11:g.841822C>T , CM000671.1:g.841822C>T GRCh37
NC_000009.10:g.831822C>T NCBI36
NG_009221.1:g.5133C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000382276.8:c.-17C>T MANE Select ENSP00000371711.3:n.-17C>T
ENST00000382276.7:c.-17C>T ENSP00000371711.3:n.-17C>T
ENST00000564322.1:n.133C>T
NM_021951.2:c.-17C>T NP_068770.2:n.-17C>T
XM_006716732.1:c.-17C>T XP_006716795.1:n.-17C>T
XM_017014375.1:c.-17C>T XP_016869864.1:n.-17C>T
NM_021951.3:c.-17C>T MANE Select NP_068770.2:n.-17C>T
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