Canonical Allele Identifier: CA187848770
Gene: DMRT1 HGNC NCBI

Linked Data

dbSNP Id: rs1047586806
gnomAD v2: 9-841787-G-C
gnomAD v3: 9-841787-G-C
gnomAD v4: 9-841787-G-C
MyVariant Identifiers: chr9:g.841787G>C (hg19) chr9:g.841787G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.841787G>C , CM000671.2:g.841787G>C GRCh38
NC_000009.11:g.841787G>C , CM000671.1:g.841787G>C GRCh37
NC_000009.10:g.831787G>C NCBI36
NG_009221.1:g.5098G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000382276.8:c.-52G>C MANE Select ENSP00000371711.3:n.-52G>C
ENST00000382276.7:c.-52G>C ENSP00000371711.3:n.-52G>C
ENST00000564322.1:n.98G>C
NM_021951.2:c.-52G>C NP_068770.2:n.-52G>C
XM_006716732.1:c.-52G>C XP_006716795.1:n.-52G>C
XM_017014375.1:c.-52G>C XP_016869864.1:n.-52G>C
NM_021951.3:c.-52G>C MANE Select NP_068770.2:n.-52G>C
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