Canonical Allele Identifier: CA12981707

Gene: NFIB

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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