Canonical Allele Identifier: CA4961393
Gene: DMRT1 HGNC NCBI

Linked Data

dbSNP Id: rs767147584
gnomAD v2: 9-841805-G-A
gnomAD v3: 9-841805-G-A
gnomAD v4: 9-841805-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.841805G>A , CM000671.2:g.841805G>A GRCh38
NC_000009.11:g.841805G>A , CM000671.1:g.841805G>A GRCh37
NC_000009.10:g.831805G>A NCBI36
NG_009221.1:g.5116G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000382276.8:c.-34G>A MANE Select ENSP00000371711.3:n.-34G>A
ENST00000382276.7:c.-34G>A ENSP00000371711.3:n.-34G>A
ENST00000564322.1:n.116G>A
NM_021951.2:c.-34G>A NP_068770.2:n.-34G>A
XM_006716732.1:c.-34G>A XP_006716795.1:n.-34G>A
XM_017014375.1:c.-34G>A XP_016869864.1:n.-34G>A
NM_021951.3:c.-34G>A MANE Select NP_068770.2:n.-34G>A