Canonical Allele Identifier: CA867712019
Gene: DMRT1 HGNC NCBI

Linked Data

dbSNP Id: rs1417035427
gnomAD v4: 9-841692-T-C
MyVariant Identifiers: chr9:g.841692T>C (hg19) chr9:g.841692T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.841692T>C , CM000671.2:g.841692T>C GRCh38
NC_000009.11:g.841692T>C , CM000671.1:g.841692T>C GRCh37
NC_000009.10:g.831692T>C NCBI36
NG_009221.1:g.5003T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000382276.7:c.-147T>C ENSP00000371711.3:n.-147T>C
ENST00000564322.1:n.3T>C
NM_021951.2:c.-147T>C NP_068770.2:n.-147T>C
XM_006716732.1:c.-147T>C XP_006716795.1:n.-147T>C
XM_017014375.1:c.-147T>C XP_016869864.1:n.-147T>C
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