Canonical Allele Identifier: CA1853838290
Gene: TMEM252-DT HGNC NCBI

Linked Data

dbSNP Id: rs1825641050

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.68578422A>G , CM000671.2:g.68578422A>G GRCh38
NC_000009.11:g.71193338A>G , CM000671.1:g.71193338A>G GRCh37
NC_000009.10:g.70383158A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_929903.1:n.449+35780A>G
XR_001746701.2:n.342+35780A>G