Canonical Allele Identifier: CA360757415
Gene: FBN2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128335227A>T , CM000667.2:g.128335227A>T GRCh38
NC_000005.9:g.127670919A>T , CM000667.1:g.127670919A>T GRCh37
NC_000005.8:g.127698818A>T NCBI36
NG_008750.1:g.207817T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000703783.1:n.700T>A
ENST00000703785.1:n.781T>A
ENST00000262464.9:c.3916T>A MANE Select ENSP00000262464.4:p.Tyr1306Asn
ENST00000262464.8:c.3916T>A ENSP00000262464.4:p.Tyr1306Asn
ENST00000507835.5:c.466T>A ENSP00000426839.1:p.Tyr156Asn
ENST00000508053.5:c.3916T>A ENSP00000424571.1:p.Tyr1306Asn
ENST00000508989.5:c.3817T>A ENSP00000425596.1:p.Tyr1273Asn
ENST00000619499.4:c.3913T>A ENSP00000482132.1:p.Tyr1305Asn
NM_001999.3:c.3916T>A NP_001990.2:p.Tyr1306Asn
XM_017009228.2:c.3763T>A XP_016864717.1:p.Tyr1255Asn
NM_001999.4:c.3916T>A MANE Select NP_001990.2:p.Tyr1306Asn