Canonical Allele Identifier: CA372774142
Gene: DMRT1 HGNC NCBI

Linked Data

dbSNP Id: rs779173960
gnomAD v4: 9-841953-G-A
MyVariant Identifiers: chr9:g.841953G>A (hg19) chr9:g.841953G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.841953G>A , CM000671.2:g.841953G>A GRCh38
NC_000009.11:g.841953G>A , CM000671.1:g.841953G>A GRCh37
NC_000009.10:g.831953G>A NCBI36
NG_009221.1:g.5264G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000382276.8:c.115G>A MANE Select ENSP00000371711.3:p.Val39Met
ENST00000382276.7:c.115G>A ENSP00000371711.3:p.Val39Met
ENST00000564322.1:n.264G>A
NM_021951.2:c.115G>A NP_068770.2:p.Val39Met
XM_006716732.1:c.115G>A XP_006716795.1:p.Val39Met
XM_017014375.1:c.115G>A XP_016869864.1:p.Val39Met
NM_021951.3:c.115G>A MANE Select NP_068770.2:p.Val39Met
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