Canonical Allele Identifier: CA1957581435

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625611C= , CM000673.2:g.22625611C= GRCh38
NC_000011.9:g.22647157C= , CM000673.1:g.22647157C= GRCh37
NC_000011.8:g.22603733C= NCBI36
NG_007425.1:g.5231G= , LRG_527:g.5231G=

Transcript Alleles

HGVS Amino-acid change
ENST00000327470.6:c.200G= (FANCF) MANE Select ENSP00000330875.3:p.Arg67=
ENST00000648096.1:n.103C= (GAS2)
ENST00000327470.4:c.200G= (FANCF) ENSP00000330875.3:p.Arg67=
NM_022725.3:c.200G= , LRG_527t1:c.200G= (FANCF) NP_073562.1:p.Arg67=
NM_022725.4:c.200G= (FANCF) MANE Select NP_073562.1:p.Arg67=