Canonical Allele Identifier: CA380059323

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625515T>A , CM000673.2:g.22625515T>A GRCh38
NC_000011.9:g.22647061T>A , CM000673.1:g.22647061T>A GRCh37
NC_000011.8:g.22603637T>A NCBI36
NG_007425.1:g.5327A>T , LRG_527:g.5327A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.296A>T (FANCF) MANE Select ENSP00000330875.3:p.Glu99Val
ENST00000648096.1:n.7T>A (GAS2)
ENST00000327470.4:c.296A>T (FANCF) ENSP00000330875.3:p.Glu99Val
NM_022725.3:c.296A>T , LRG_527t1:c.296A>T (FANCF) NP_073562.1:p.Glu99Val
NM_022725.4:c.296A>T (FANCF) MANE Select NP_073562.1:p.Glu99Val