Canonical Allele Identifier: CA4961390
Gene: DMRT1 HGNC NCBI

Linked Data

dbSNP Id: rs763517922
ExAC: 9:841796 CGA / C
gnomAD v2: 9-841796-CGA-C
gnomAD v3: 9-841796-CGA-C
gnomAD v4: 9-841796-CGA-C
MyVariant Identifiers: chr9:g.841797_841798del (hg19) chr9:g.841797_841798del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.841802_841803del , CM000671.2:g.841802_841803del GRCh38
NC_000009.11:g.841802_841803del , CM000671.1:g.841802_841803del GRCh37
NC_000009.10:g.831802_831803del NCBI36
NG_009221.1:g.5113_5114del

Transcript Alleles

HGVS Amino-acid change
ENST00000382276.8:c.-37_-36del MANE Select ENSP00000371711.3:n.-37_-36del
ENST00000382276.7:c.-37_-36del ENSP00000371711.3:n.-37_-36del
ENST00000564322.1:n.113_114del
NM_021951.2:c.-37_-36del NP_068770.2:n.-37_-36del
XM_006716732.1:c.-37_-36del XP_006716795.1:n.-37_-36del
XM_017014375.1:c.-37_-36del XP_016869864.1:n.-37_-36del
NM_021951.3:c.-37_-36del MANE Select NP_068770.2:n.-37_-36del
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