Canonical Allele Identifier: CA4961436
Gene: DMRT1 HGNC NCBI

Linked Data

dbSNP Id: rs370275067
gnomAD v2: 9-841934-C-T
gnomAD v3: 9-841934-C-T
gnomAD v4: 9-841934-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.841934C>T , CM000671.2:g.841934C>T GRCh38
NC_000009.11:g.841934C>T , CM000671.1:g.841934C>T GRCh37
NC_000009.10:g.831934C>T NCBI36
NG_009221.1:g.5245C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000382276.8:c.96C>T MANE Select ENSP00000371711.3:p.Gly32=
ENST00000382276.7:c.96C>T ENSP00000371711.3:p.Gly32=
ENST00000564322.1:n.245C>T
NM_021951.2:c.96C>T NP_068770.2:p.Gly32=
XM_006716732.1:c.96C>T XP_006716795.1:p.Gly32=
XM_017014375.1:c.96C>T XP_016869864.1:p.Gly32=
NM_021951.3:c.96C>T MANE Select NP_068770.2:p.Gly32=