Canonical Allele Identifier: CA2597403531
Gene: TMEM252-DT HGNC NCBI

Linked Data

dbSNP Id: rs2132149839
gnomAD v3: 9-68578232-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.68578232T>A , CM000671.2:g.68578232T>A GRCh38
NC_000009.11:g.71193148T>A , CM000671.1:g.71193148T>A GRCh37
NC_000009.10:g.70382968T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_929903.1:n.449+35590T>A
XR_001746701.2:n.342+35590T>A