Canonical Allele Identifier: CA360759428
Gene: FBN2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128338078T>C , CM000667.2:g.128338078T>C GRCh38
NC_000005.9:g.127673770T>C , CM000667.1:g.127673770T>C GRCh37
NC_000005.8:g.127701669T>C NCBI36
NG_008750.1:g.204966A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000703783.1:n.301A>G
ENST00000703785.1:n.382A>G
ENST00000262464.9:c.3517A>G MANE Select ENSP00000262464.4:p.Thr1173Ala
ENST00000262464.8:c.3517A>G ENSP00000262464.4:p.Thr1173Ala
ENST00000507835.5:c.67A>G ENSP00000426839.1:p.Thr23Ala
ENST00000508053.5:c.3517A>G ENSP00000424571.1:p.Thr1173Ala
ENST00000508989.5:c.3418A>G ENSP00000425596.1:p.Thr1140Ala
ENST00000619499.4:c.3514A>G ENSP00000482132.1:p.Thr1172Ala
NM_001999.3:c.3517A>G NP_001990.2:p.Thr1173Ala
XM_017009228.2:c.3364A>G XP_016864717.1:p.Thr1122Ala
NM_001999.4:c.3517A>G MANE Select NP_001990.2:p.Thr1173Ala