Canonical Allele Identifier: CA1853838228
Gene: TMEM252-DT HGNC NCBI

Linked Data

dbSNP Id: rs1825639734

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.68578260G>A , CM000671.2:g.68578260G>A GRCh38
NC_000009.11:g.71193176G>A , CM000671.1:g.71193176G>A GRCh37
NC_000009.10:g.70382996G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_929903.1:n.449+35618G>A
XR_001746701.2:n.342+35618G>A