Allele Registry

Canonical Allele Identifier: CA15414718

Gene: NSG2 HGNC NCBI

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr5:g.174198151T>C

GRCh37 chr5:g.173625154T>C

Linked Data - Sequence & Population

gnomAD v2:

5:173625154 T / C

gnomAD v3:

5:174198151 T / C

gnomAD v4:

chr5-174198151-T-C

Joint Max Group AF 0.87665024 (EAS)

Genomes Max Group AF 0.87665024 (EAS)

Linked Data - NCBI & NCI

dbSNP:

6863418

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.174198151T>C , CM000667.2:g.174198151T>C	GRCh38
NC_000005.9:g.173625154T>C , CM000667.1:g.173625154T>C	GRCh37
NC_000005.8:g.173557760T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000521585.5:c.214-7049T>C	ENSP00000429863.1:n.214-7049T>C

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