Canonical Allele Identifier: CA11604047
Gene: FHIT HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10510837

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.60304113G>A , CM000665.2:g.60304113G>A GRCh38
NC_000003.10:g.60264882G>A NCBI36
NC_000003.11:g.60289842G>A , CM000665.1:g.60289842G>A GRCh37
NG_007551.1:g.952292C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000468189.5:c.103+232747C>T ENSP00000417480.1:p.=
ENST00000476844.5:c.103+232747C>T ENSP00000417557.1:p.=
ENST00000488467.5:c.103+232747C>T ENSP00000418596.1:p.=
ENST00000492590.5:c.103+232747C>T ENSP00000418582.1:p.=
NM_001166243.1:c.103+232747C>T NP_001159715.1:p.=
NM_002012.2:c.103+232747C>T NP_002003.1:p.=
XM_011533481.1:c.103+232747C>T XP_011531783.1:p.=
XM_011533482.1:c.103+232747C>T XP_011531784.1:p.=
XM_011533483.1:c.103+232747C>T XP_011531785.1:p.=
XM_011533484.1:c.103+232747C>T XP_011531786.1:p.=
XM_011533485.1:c.103+232747C>T XP_011531787.1:p.=
XM_011533486.1:c.103+232747C>T XP_011531788.1:p.=