Canonical Allele Identifier: CA196564488
Community Standard Title: NM_000507.4(FBP1):c.206A>G (p.Asp69Gly)
Gene: FBP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94620456T>C , CM000671.2:g.94620456T>C GRCh38
NC_000009.11:g.97382738T>C , CM000671.1:g.97382738T>C GRCh37
NC_000009.10:g.96422559T>C NCBI36
NG_008174.1:g.24794A>G

Transcript Alleles

HGVS Amino-acid Change
NM_000507.4:c.206A>G MANE Select NP_000498.2:p.Asp69Gly
ENST00000375326.9:c.206A>G MANE Select ENSP00000364475.5:p.Asp69Gly
NM_000507.3:c.206A>G NP_000498.2:p.Asp69Gly
NM_001127628.1:c.206A>G NP_001121100.1:p.Asp69Gly
NM_001127628.2:c.206A>G NP_001121100.1:p.Asp69Gly
ENST00000375326.8:c.206A>G ENSP00000364475.4:p.Asp69Gly
ENST00000414122.1:c.-47A>G ENSP00000411619.1:n.-47A>G
ENST00000415431.5:c.206A>G ENSP00000408025.1:p.Asp69Gly
ENST00000648117.1:c.104A>G ENSP00000498145.1:p.Asp35Gly
ENST00000682520.1:c.206A>G ENSP00000507547.1:p.Asp69Gly
XM_006717005.2:c.-41A>G XP_006717068.1:n.-41A>G
XM_006717005.4:c.-41A>G XP_006717068.1:n.-41A>G