Canonical Allele Identifier: CA1957581440

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625619G= , CM000673.2:g.22625619G= GRCh38
NC_000011.9:g.22647165G= , CM000673.1:g.22647165G= GRCh37
NC_000011.8:g.22603741G= NCBI36
NG_007425.1:g.5223C= , LRG_527:g.5223C=

Transcript Alleles

HGVS Amino-acid change
ENST00000327470.6:c.192C= (FANCF) MANE Select ENSP00000330875.3:p.Asn64=
ENST00000648096.1:n.111G= (GAS2)
ENST00000327470.4:c.192C= (FANCF) ENSP00000330875.3:p.Asn64=
NM_022725.3:c.192C= , LRG_527t1:c.192C= (FANCF) NP_073562.1:p.Asn64=
NM_022725.4:c.192C= (FANCF) MANE Select NP_073562.1:p.Asn64=