Canonical Allele Identifier: CA585900998
Gene: DMRT1 HGNC NCBI

Linked Data

dbSNP Id: rs1316886735
gnomAD v2: 9-841701-C-T
gnomAD v3: 9-841701-C-T
gnomAD v4: 9-841701-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.841701C>T , CM000671.2:g.841701C>T GRCh38
NC_000009.11:g.841701C>T , CM000671.1:g.841701C>T GRCh37
NC_000009.10:g.831701C>T NCBI36
NG_009221.1:g.5012C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000382276.8:c.-138C>T MANE Select ENSP00000371711.3:n.-138C>T
ENST00000382276.7:c.-138C>T ENSP00000371711.3:n.-138C>T
ENST00000564322.1:n.12C>T
NM_021951.2:c.-138C>T NP_068770.2:n.-138C>T
XM_006716732.1:c.-138C>T XP_006716795.1:n.-138C>T
XM_017014375.1:c.-138C>T XP_016869864.1:n.-138C>T
NM_021951.3:c.-138C>T MANE Select NP_068770.2:n.-138C>T