Canonical Allele Identifier: CA1835002799
Gene: NFIB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.14446003C= , CM000671.2:g.14446003C= GRCh38
NC_000009.11:g.14446001C= , CM000671.1:g.14446001C= GRCh37
NC_000009.10:g.14436001C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001369458.1:c.96+85944G= NP_001356387.1:n.96+85944G=
NM_001369459.1:c.96+85944G= NP_001356388.1:n.96+85944G=
NM_001369462.1:c.96+85944G= NP_001356391.1:n.96+85944G=
NM_001369468.1:c.96+85944G= NP_001356397.1:n.96+85944G=