Canonical Allele Identifier: CA1619326122
Gene: SNHG32 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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