Canonical Allele Identifier: CA866233780
Gene: TMEM252-DT HGNC NCBI

Linked Data

dbSNP Id: rs1294617805
MyVariant Identifiers: chr9:g.71193264T>C (hg19) chr9:g.68578348T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.68578348T>C , CM000671.2:g.68578348T>C GRCh38
NC_000009.11:g.71193264T>C , CM000671.1:g.71193264T>C GRCh37
NC_000009.10:g.70383084T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_929903.1:n.449+35706T>C
XR_001746701.2:n.342+35706T>C
Search 100 bp 5'
Search 100 bp 3'