Canonical Allele Identifier: CA1084574581

Gene: NSG2

Linked Data

• dbSNP Id: rs1755679274
• gnomAD v3: 5-174221407-G-C
• gnomAD v4: 5-174221407-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.174221407G>C , CM000667.2:g.174221407G>C	GRCh38
NC_000005.9:g.173648410G>C , CM000667.1:g.173648410G>C	GRCh37
NC_000005.8:g.173581016G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000521585.5:c.*18+16103G>C	ENSP00000429863.1:n.*18+16103G>C