Canonical Allele Identifier: CA4961648

Gene: DMRT1

Linked Data

• ClinVar Variation Id: 786903
• ClinVar RCV Id: RCV000969039
• dbSNP Id: rs146975077
• ExAC: 9:894147 G / C
• gnomAD v2: 9-894147-G-C
• gnomAD v3: 9-894147-G-C
• gnomAD v4: 9-894147-G-C
• MyVariant Identifiers: chr9:g.894147G>C (hg19) ; chr9:g.894147G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.894147G>C , CM000671.2:g.894147G>C	GRCh38
NC_000009.11:g.894147G>C , CM000671.1:g.894147G>C	GRCh37
NC_000009.10:g.884147G>C	NCBI36
NG_009221.1:g.57458G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382276.8:c.774G>C MANE Select	ENSP00000371711.3:p.Arg258=
ENST00000382276.7:c.774G>C	ENSP00000371711.3:p.Arg258=
ENST00000564322.1:n.923G>C
ENST00000569227.1:c.300G>C	ENSP00000454701.1:p.Arg100=
NM_021951.2:c.774G>C	NP_068770.2:p.Arg258=
XM_006716732.1:c.774G>C	XP_006716795.1:p.Arg258=
XM_011517770.1:c.822G>C	XP_011516072.1:p.Arg274=
XM_011517771.1:c.822G>C	XP_011516073.1:p.Arg274=
XM_011517772.1:c.822G>C	XP_011516074.1:p.Arg274=
XM_011517773.1:c.300G>C	XP_011516075.1:p.Arg100=
NM_001363767.1:c.300G>C	NP_001350696.1:p.Arg100=
XM_011517773.3:c.300G>C	XP_011516075.1:p.Arg100=
XM_017014374.1:c.587-22616G>C	XP_016869863.1:n.587-22616G>C
XM_017014375.1:c.539-22616G>C	XP_016869864.1:n.539-22616G>C
XM_024447434.1:c.228G>C	XP_024303202.1:p.Arg76=
NM_021951.3:c.774G>C MANE Select	NP_068770.2:p.Arg258=