Canonical Allele Identifier: CA2318792887
Gene: NFIC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3318512A= , CM000681.2:g.3318512A= GRCh38
NC_000019.9:g.3318510A= , CM000681.1:g.3318510A= GRCh37
NC_000019.8:g.3269510A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000641145.1:c.96+3656A= ENSP00000492983.1:n.96+3656A=