Canonical Allele Identifier: CA4961762
Gene: DMRT1 HGNC NCBI
COSMIC:
COSN20055032 (not active)
MyVariant.info:
GRCh38 chr9:g.967959T>C
GRCh37 chr9:g.967959T>C
gnomAD v2:
9:967959 T / C
gnomAD v3:
9:967959 T / C
gnomAD v4:
chr9-967959-T-C
Joint Max Group AF 0.0001612 (AFR)
Genomes Max Group AF 0.00024072 (AFR)
Exomes Max Group AF 0.00002378 (AFR)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.967959T>C , CM000671.2:g.967959T>C GRCh38
NC_000009.11:g.967959T>C , CM000671.1:g.967959T>C GRCh37
NC_000009.10:g.957959T>C NCBI36
NG_009221.1:g.131270T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000382276.8:c.968-26T>C MANE Select ENSP00000371711.3:n.968-26T>C
ENST00000382276.7:c.968-26T>C ENSP00000371711.3:n.968-26T>C
ENST00000569227.1:c.494-26T>C ENSP00000454701.1:n.494-26T>C
NM_021951.2:c.968-26T>C NP_068770.2:n.968-26T>C
XM_006716732.1:c.971-26T>C XP_006716795.1:n.971-26T>C
XM_011517770.1:c.1019-26T>C XP_011516072.1:n.1019-26T>C
XM_011517771.1:c.1016-26T>C XP_011516073.1:n.1016-26T>C
XM_011517772.1:c.871-26T>C XP_011516074.1:n.871-26T>C
XM_011517773.1:c.497-26T>C XP_011516075.1:n.497-26T>C
NM_001363767.1:c.494-26T>C NP_001350696.1:n.494-26T>C
XM_011517773.3:c.497-26T>C XP_011516075.1:n.497-26T>C
XM_017014374.1:c.*36-26T>C XP_016869863.1:n.*36-26T>C
XM_017014375.1:c.*36-26T>C XP_016869864.1:n.*36-26T>C
XM_024447434.1:c.422-26T>C XP_024303202.1:n.422-26T>C
NM_021951.3:c.968-26T>C MANE Select NP_068770.2:n.968-26T>C
Search 100 bp 5'
Search 100 bp 3'