Canonical Allele Identifier: CA4961412
Gene: DMRT1 HGNC NCBI

Linked Data

dbSNP Id: rs572998698
ExAC: 9:841868 C / T
gnomAD v2: 9-841868-C-T
gnomAD v4: 9-841868-C-T
MyVariant Identifiers: chr9:g.841868C>T (hg19) chr9:g.841868C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.841868C>T , CM000671.2:g.841868C>T GRCh38
NC_000009.11:g.841868C>T , CM000671.1:g.841868C>T GRCh37
NC_000009.10:g.831868C>T NCBI36
NG_009221.1:g.5179C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000382276.8:c.30C>T MANE Select ENSP00000371711.3:p.Pro10=
ENST00000382276.7:c.30C>T ENSP00000371711.3:p.Pro10=
ENST00000564322.1:n.179C>T
NM_021951.2:c.30C>T NP_068770.2:p.Pro10=
XM_006716732.1:c.30C>T XP_006716795.1:p.Pro10=
XM_017014375.1:c.30C>T XP_016869864.1:p.Pro10=
NM_021951.3:c.30C>T MANE Select NP_068770.2:p.Pro10=
Search 100 bp 5'
Search 100 bp 3'