Canonical Allele Identifier: CA12231348
Gene: SNHG32 HGNC NCBI

Linked Data

dbSNP Id: rs9368699
gnomAD v2: 6-31802541-T-C
gnomAD v3: 6-31834764-T-C
gnomAD v4: 6-31834764-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31834764T>C , CM000668.2:g.31834764T>C GRCh38
NC_000006.11:g.31802541T>C , CM000668.1:g.31802541T>C GRCh37
NC_000006.10:g.31910520T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000375640.7:c.-571T>C ENSP00000364791.3:n.-571T>C
ENST00000375641.6:c.-139T>C ENSP00000364792.2:n.-139T>C