Canonical Allele Identifier: CA1162048282
Gene: SMIM12 HGNC NCBI

Linked Data

dbSNP Id: rs1640610678

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34823512del , CM000663.2:g.34823512del GRCh38
NC_000001.10:g.35289113del , CM000663.1:g.35289113del GRCh37
NC_000001.9:g.35061700del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000426886.1:c.207+32259del ENSP00000429902.1:n.207+32259del