Canonical Allele Identifier: CA4961387
Gene: DMRT1 HGNC NCBI

Linked Data

dbSNP Id: rs777110890
gnomAD v2: 9-841789-C-G
gnomAD v4: 9-841789-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.841789C>G , CM000671.2:g.841789C>G GRCh38
NC_000009.11:g.841789C>G , CM000671.1:g.841789C>G GRCh37
NC_000009.10:g.831789C>G NCBI36
NG_009221.1:g.5100C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000382276.8:c.-50C>G MANE Select ENSP00000371711.3:n.-50C>G
ENST00000382276.7:c.-50C>G ENSP00000371711.3:n.-50C>G
ENST00000564322.1:n.100C>G
NM_021951.2:c.-50C>G NP_068770.2:n.-50C>G
XM_006716732.1:c.-50C>G XP_006716795.1:n.-50C>G
XM_017014375.1:c.-50C>G XP_016869864.1:n.-50C>G
NM_021951.3:c.-50C>G MANE Select NP_068770.2:n.-50C>G