Canonical Allele Identifier: CA1162048266
Gene: SMIM12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34823481A= , CM000663.2:g.34823481A= GRCh38
NC_000001.10:g.35289082A= , CM000663.1:g.35289082A= GRCh37
NC_000001.9:g.35061669A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000426886.1:c.207+32290T= ENSP00000429902.1:n.207+32290T=