Canonical Allele Identifier: CA1000448645
Gene: SMIM12 HGNC NCBI

Linked Data

dbSNP Id: rs1640609363
gnomAD v3: 1-34823338-A-G
gnomAD v4: 1-34823338-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34823338A>G , CM000663.2:g.34823338A>G GRCh38
NC_000001.10:g.35288939A>G , CM000663.1:g.35288939A>G GRCh37
NC_000001.9:g.35061526A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000426886.1:c.207+32433T>C ENSP00000429902.1:n.207+32433T>C