Canonical Allele Identifier: CA735290964
Gene: SMIM12 HGNC NCBI

Linked Data

dbSNP Id: rs1211564441

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34823389T>C , CM000663.2:g.34823389T>C GRCh38
NC_000001.10:g.35288990T>C , CM000663.1:g.35288990T>C GRCh37
NC_000001.9:g.35061577T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000426886.1:c.207+32382A>G ENSP00000429902.1:n.207+32382A>G