Canonical Allele Identifier: CA735290967
Gene: SMIM12 HGNC NCBI

Linked Data

dbSNP Id: rs1252091908

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34823392T>G , CM000663.2:g.34823392T>G GRCh38
NC_000001.10:g.35288993T>G , CM000663.1:g.35288993T>G GRCh37
NC_000001.9:g.35061580T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000426886.1:c.207+32379A>C ENSP00000429902.1:n.207+32379A>C