Canonical Allele Identifier: CA1853838226
Gene: TMEM252-DT HGNC NCBI

Linked Data

dbSNP Id: rs1825639714

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.68578259A>G , CM000671.2:g.68578259A>G GRCh38
NC_000009.11:g.71193175A>G , CM000671.1:g.71193175A>G GRCh37
NC_000009.10:g.70382995A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_929903.1:n.449+35617A>G
XR_001746701.2:n.342+35617A>G