Canonical Allele Identifier: CA1084574657

Gene: NSG2

Linked Data

• dbSNP Id: rs1755682173
• gnomAD v3: 5-174221703-G-C
• gnomAD v4: 5-174221703-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.174221703G>C , CM000667.2:g.174221703G>C	GRCh38
NC_000005.9:g.173648706G>C , CM000667.1:g.173648706G>C	GRCh37
NC_000005.8:g.173581312G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000521585.5:c.*18+16399G>C	ENSP00000429863.1:n.*18+16399G>C