Canonical Allele Identifier: CA2123502298
Community Standard Title: NC_000014.9:g.23507801A=
Gene: NGDN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23507801A= , CM000676.2:g.23507801A= GRCh38
NC_000014.8:g.23977010A= , CM000676.1:g.23977010A= GRCh37
NC_000014.7:g.23046850A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000556699.1:c.203-1539A= ENSP00000451942.1:n.203-1539A=
ENST00000556699.2:c.929-1539A= ENSP00000451942.2:n.929-1539A=
ENST00000703257.1:c.871-1539A= ENSP00000515246.1:n.871-1539A=