Canonical Allele Identifier: CA1801471646
Community Standard Title: NC_000008.11:g.89985681A=
Gene: NBN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.89985681A= , CM000670.2:g.89985681A= GRCh38
NC_000008.10:g.90997909A= , CM000670.1:g.90997909A= GRCh37
NC_000008.9:g.91067085A= NCBI36
NG_008860.1:g.3991T= , LRG_158:g.3991T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000396252.6:c.-229-708T= ENSP00000379551.2:n.-229-708T=