Canonical Allele Identifier: CA1162048274
Gene: SMIM12 HGNC NCBI

Linked Data

dbSNP Id: rs1640610590

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34823494T>C , CM000663.2:g.34823494T>C GRCh38
NC_000001.10:g.35289095T>C , CM000663.1:g.35289095T>C GRCh37
NC_000001.9:g.35061682T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000426886.1:c.207+32277A>G ENSP00000429902.1:n.207+32277A>G