Canonical Allele Identifier: CA1162048229
Gene: SMIM12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34823373G= , CM000663.2:g.34823373G= GRCh38
NC_000001.10:g.35288974G= , CM000663.1:g.35288974G= GRCh37
NC_000001.9:g.35061561G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000426886.1:c.207+32398C= ENSP00000429902.1:n.207+32398C=