Canonical Allele Identifier: CA867712031
Gene: DMRT1 HGNC NCBI

Linked Data

dbSNP Id: rs1479664989
gnomAD v4: 9-841728-C-G
MyVariant Identifiers: chr9:g.841728C>G (hg19) chr9:g.841728C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.841728C>G , CM000671.2:g.841728C>G GRCh38
NC_000009.11:g.841728C>G , CM000671.1:g.841728C>G GRCh37
NC_000009.10:g.831728C>G NCBI36
NG_009221.1:g.5039C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000382276.8:c.-111C>G MANE Select ENSP00000371711.3:n.-111C>G
ENST00000382276.7:c.-111C>G ENSP00000371711.3:n.-111C>G
ENST00000564322.1:n.39C>G
NM_021951.2:c.-111C>G NP_068770.2:n.-111C>G
XM_006716732.1:c.-111C>G XP_006716795.1:n.-111C>G
XM_017014375.1:c.-111C>G XP_016869864.1:n.-111C>G
NM_021951.3:c.-111C>G MANE Select NP_068770.2:n.-111C>G
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