Allele Registry

Canonical Allele Identifier: CA14651940

Gene: NFIC HGNC NCBI

MyVariant.info:

GRCh38 chr19:g.3318512A>G

GRCh37 chr19:g.3318510A>G

gnomAD v2:

19:3318510 A / G

gnomAD v3:

19:3318512 A / G

gnomAD v4:

chr19-3318512-A-G

Joint Max Group AF 0.5452013 (NFE)

Genomes Max Group AF 0.5452013 (NFE)

dbSNP:

11669592

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