Canonical Allele Identifier: CA372773899
Gene: DMRT1 HGNC NCBI

Linked Data

dbSNP Id: rs1373161239
gnomAD v2: 9-841869-T-C
MyVariant Identifiers: chr9:g.841869T>C (hg19) chr9:g.841869T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.841869T>C , CM000671.2:g.841869T>C GRCh38
NC_000009.11:g.841869T>C , CM000671.1:g.841869T>C GRCh37
NC_000009.10:g.831869T>C NCBI36
NG_009221.1:g.5180T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000382276.8:c.31T>C MANE Select ENSP00000371711.3:p.Ser11Pro
ENST00000382276.7:c.31T>C ENSP00000371711.3:p.Ser11Pro
ENST00000564322.1:n.180T>C
NM_021951.2:c.31T>C NP_068770.2:p.Ser11Pro
XM_006716732.1:c.31T>C XP_006716795.1:p.Ser11Pro
XM_017014375.1:c.31T>C XP_016869864.1:p.Ser11Pro
NM_021951.3:c.31T>C MANE Select NP_068770.2:p.Ser11Pro
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