Canonical Allele Identifier: CA4961388
Gene: DMRT1 HGNC NCBI

Linked Data

dbSNP Id: rs763201923
ExAC: 9:841790 T / C
gnomAD v2: 9-841790-T-C
gnomAD v4: 9-841790-T-C
MyVariant Identifiers: chr9:g.841790T>C (hg19) chr9:g.841790T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.841790T>C , CM000671.2:g.841790T>C GRCh38
NC_000009.11:g.841790T>C , CM000671.1:g.841790T>C GRCh37
NC_000009.10:g.831790T>C NCBI36
NG_009221.1:g.5101T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000382276.8:c.-49T>C MANE Select ENSP00000371711.3:n.-49T>C
ENST00000382276.7:c.-49T>C ENSP00000371711.3:n.-49T>C
ENST00000564322.1:n.101T>C
NM_021951.2:c.-49T>C NP_068770.2:n.-49T>C
XM_006716732.1:c.-49T>C XP_006716795.1:n.-49T>C
XM_017014375.1:c.-49T>C XP_016869864.1:n.-49T>C
NM_021951.3:c.-49T>C MANE Select NP_068770.2:n.-49T>C
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