Canonical Allele Identifier: CA372773886
Gene: DMRT1 HGNC NCBI

Linked Data

dbSNP Id: rs139583942
MyVariant Identifiers: chr9:g.841866C>A (hg19) chr9:g.841866C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.841866C>A , CM000671.2:g.841866C>A GRCh38
NC_000009.11:g.841866C>A , CM000671.1:g.841866C>A GRCh37
NC_000009.10:g.831866C>A NCBI36
NG_009221.1:g.5177C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000382276.8:c.28C>A MANE Select ENSP00000371711.3:p.Pro10Thr
ENST00000382276.7:c.28C>A ENSP00000371711.3:p.Pro10Thr
ENST00000564322.1:n.177C>A
NM_021951.2:c.28C>A NP_068770.2:p.Pro10Thr
XM_006716732.1:c.28C>A XP_006716795.1:p.Pro10Thr
XM_017014375.1:c.28C>A XP_016869864.1:p.Pro10Thr
NM_021951.3:c.28C>A MANE Select NP_068770.2:p.Pro10Thr
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