Canonical Allele Identifier: CA1835010922
Community Standard Title: NC_000009.12:g.14470835A=
Gene: NFIB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.14470835A= , CM000671.2:g.14470835A= GRCh38
NC_000009.11:g.14470833A= , CM000671.1:g.14470833A= GRCh37
NC_000009.10:g.14460833A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001369458.1:c.96+61112T= NP_001356387.1:n.96+61112T=
NM_001369459.1:c.96+61112T= NP_001356388.1:n.96+61112T=
NM_001369462.1:c.96+61112T= NP_001356391.1:n.96+61112T=
NM_001369468.1:c.96+61112T= NP_001356397.1:n.96+61112T=