Canonical Allele Identifier: CA1000448676
Gene: SMIM12 HGNC NCBI

Linked Data

dbSNP Id: rs1460386769
gnomAD v3: 1-34823443-T-G
gnomAD v4: 1-34823443-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34823443T>G , CM000663.2:g.34823443T>G GRCh38
NC_000001.10:g.35289044T>G , CM000663.1:g.35289044T>G GRCh37
NC_000001.9:g.35061631T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000426886.1:c.207+32328A>C ENSP00000429902.1:n.207+32328A>C