Canonical Allele Identifier: CA1162048284
Gene: SMIM12 HGNC NCBI

Linked Data

dbSNP Id: rs1640610691

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34823513T>C , CM000663.2:g.34823513T>C GRCh38
NC_000001.10:g.35289114T>C , CM000663.1:g.35289114T>C GRCh37
NC_000001.9:g.35061701T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000426886.1:c.207+32258A>G ENSP00000429902.1:n.207+32258A>G