Canonical Allele Identifier: CA645881705
Gene: SMIM12 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34823412C>A , CM000663.2:g.34823412C>A GRCh38
NC_000001.10:g.35289013C>A , CM000663.1:g.35289013C>A GRCh37
NC_000001.9:g.35061600C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000426886.1:c.207+32359G>T ENSP00000429902.1:n.207+32359G>T