Canonical Allele Identifier: CA866233702
Gene: TMEM252-DT HGNC NCBI

Linked Data

dbSNP Id: rs1240066539
gnomAD v3: 9-68578182-C-G
gnomAD v4: 9-68578182-C-G
MyVariant Identifiers: chr9:g.71193098C>G (hg19) chr9:g.68578182C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.68578182C>G , CM000671.2:g.68578182C>G GRCh38
NC_000009.11:g.71193098C>G , CM000671.1:g.71193098C>G GRCh37
NC_000009.10:g.70382918C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_929903.1:n.449+35540C>G
XR_001746701.2:n.342+35540C>G
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