Canonical Allele Identifier: CA360753792
Gene: FBN2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128330575G>T , CM000667.2:g.128330575G>T GRCh38
NC_000005.9:g.127666267G>T , CM000667.1:g.127666267G>T GRCh37
NC_000005.8:g.127694166G>T NCBI36
NG_008750.1:g.212469C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000703783.1:n.1127C>A
ENST00000703785.1:n.1208C>A
ENST00000262464.9:c.4343C>A MANE Select ENSP00000262464.4:p.Ser1448Ter
ENST00000262464.8:c.4343C>A ENSP00000262464.4:p.Ser1448Ter
ENST00000507835.5:c.893C>A ENSP00000426839.1:p.Ser298Ter
ENST00000508053.5:c.4343C>A ENSP00000424571.1:p.Ser1448Ter
ENST00000508989.5:c.4244C>A ENSP00000425596.1:p.Ser1415Ter
ENST00000619499.4:c.4340C>A ENSP00000482132.1:p.Ser1447Ter
NM_001999.3:c.4343C>A NP_001990.2:p.Ser1448Ter
XM_017009228.2:c.4190C>A XP_016864717.1:p.Ser1397Ter
NM_001999.4:c.4343C>A MANE Select NP_001990.2:p.Ser1448Ter