Canonical Allele Identifier: CA1602103139
Gene: NSG2 HGNC NCBI

Linked Data

dbSNP Id: rs1755678063
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174221298C>A , CM000667.2:g.174221298C>A GRCh38
NC_000005.9:g.173648301C>A , CM000667.1:g.173648301C>A GRCh37
NC_000005.8:g.173580907C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521585.5:c.*18+15994C>A ENSP00000429863.1:n.*18+15994C>A
Search 100 bp 5'
Search 100 bp 3'