Canonical Allele Identifier: CA14651940
Gene: NFIC HGNC NCBI

Linked Data

dbSNP Id: rs11669592
gnomAD v2: 19-3318510-A-G
gnomAD v3: 19-3318512-A-G
gnomAD v4: 19-3318512-A-G
MyVariant Identifiers: chr19:g.3318510A>G (hg19) chr19:g.3318512A>G (hg38)
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Genomic Alleles

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

Transcript Alleles

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