Canonical Allele Identifier: CA181286528

Gene: NBN

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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