Canonical Allele Identifier: CA588310940
Gene: TMEM252-DT HGNC NCBI

Linked Data

dbSNP Id: rs1432337750
gnomAD v2: 9-71193277-C-A
gnomAD v3: 9-68578361-C-A
gnomAD v4: 9-68578361-C-A
MyVariant Identifiers: chr9:g.71193277C>A (hg19) chr9:g.68578361C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.68578361C>A , CM000671.2:g.68578361C>A GRCh38
NC_000009.11:g.71193277C>A , CM000671.1:g.71193277C>A GRCh37
NC_000009.10:g.70383097C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_929903.1:n.449+35719C>A
XR_001746701.2:n.342+35719C>A
Search 100 bp 5'
Search 100 bp 3'