Canonical Allele Identifier: CA1162048278
Gene: SMIM12 HGNC NCBI

Linked Data

dbSNP Id: rs1640610633

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34823498C>G , CM000663.2:g.34823498C>G GRCh38
NC_000001.10:g.35289099C>G , CM000663.1:g.35289099C>G GRCh37
NC_000001.9:g.35061686C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000426886.1:c.207+32273G>C ENSP00000429902.1:n.207+32273G>C