Canonical Allele Identifier: CA12231348
Gene: SNHG32 HGNC NCBI
MyVariant.info:
GRCh38 chr6:g.31834764T>C
GRCh37 chr6:g.31802541T>C
gnomAD v2:
6:31802541 T / C
gnomAD v3:
6:31834764 T / C
gnomAD v4:
chr6-31834764-T-C
Joint Max Group AF 0.16994979 (EAS)
Genomes Max Group AF 0.17693238 (EAS)
Exomes Max Group AF 0.16147364 (EAS)
dbSNP:
9368699
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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
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