Canonical Allele Identifier: CA2606454025

Gene: NSG2

Linked Data

• dbSNP Id: rs2113100815
• gnomAD v3: 5-174221512-T-C
• gnomAD v4: 5-174221512-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.174221512T>C , CM000667.2:g.174221512T>C	GRCh38
NC_000005.9:g.173648515T>C , CM000667.1:g.173648515T>C	GRCh37
NC_000005.8:g.173581121T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000521585.5:c.*18+16208T>C	ENSP00000429863.1:n.*18+16208T>C