Canonical Allele Identifier: CA360753816
Gene: FBN2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128330579A>C , CM000667.2:g.128330579A>C GRCh38
NC_000005.9:g.127666271A>C , CM000667.1:g.127666271A>C GRCh37
NC_000005.8:g.127694170A>C NCBI36
NG_008750.1:g.212465T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000703783.1:n.1123T>G
ENST00000703785.1:n.1204T>G
ENST00000262464.9:c.4339T>G MANE Select ENSP00000262464.4:p.Cys1447Gly
ENST00000262464.8:c.4339T>G ENSP00000262464.4:p.Cys1447Gly
ENST00000507835.5:c.889T>G ENSP00000426839.1:p.Cys297Gly
ENST00000508053.5:c.4339T>G ENSP00000424571.1:p.Cys1447Gly
ENST00000508989.5:c.4240T>G ENSP00000425596.1:p.Cys1414Gly
ENST00000619499.4:c.4336T>G ENSP00000482132.1:p.Cys1446Gly
NM_001999.3:c.4339T>G NP_001990.2:p.Cys1447Gly
XM_017009228.2:c.4186T>G XP_016864717.1:p.Cys1396Gly
NM_001999.4:c.4339T>G MANE Select NP_001990.2:p.Cys1447Gly