Canonical Allele Identifier: CA1084574570

Gene: NSG2

Linked Data

• dbSNP Id: rs1755679156
• gnomAD v3: 5-174221382-G-C
• gnomAD v4: 5-174221382-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.174221382G>C , CM000667.2:g.174221382G>C	GRCh38
NC_000005.9:g.173648385G>C , CM000667.1:g.173648385G>C	GRCh37
NC_000005.8:g.173580991G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000521585.5:c.*18+16078G>C	ENSP00000429863.1:n.*18+16078G>C