Canonical Allele Identifier: CA360753938

Gene: FBN2

Linked Data

• MyVariant Identifiers: chr5:g.127666300G>C (hg19) ; chr5:g.128330608G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128330608G>C , CM000667.2:g.128330608G>C	GRCh38
NC_000005.9:g.127666300G>C , CM000667.1:g.127666300G>C	GRCh37
NC_000005.8:g.127694199G>C	NCBI36
NG_008750.1:g.212436C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000703783.1:n.1094C>G
ENST00000703785.1:n.1175C>G
ENST00000262464.9:c.4310C>G MANE Select	ENSP00000262464.4:p.Ser1437Cys
ENST00000262464.8:c.4310C>G	ENSP00000262464.4:p.Ser1437Cys
ENST00000507835.5:c.860C>G	ENSP00000426839.1:p.Ser287Cys
ENST00000508053.5:c.4310C>G	ENSP00000424571.1:p.Ser1437Cys
ENST00000508989.5:c.4211C>G	ENSP00000425596.1:p.Ser1404Cys
ENST00000619499.4:c.4307C>G	ENSP00000482132.1:p.Ser1436Cys
NM_001999.3:c.4310C>G	NP_001990.2:p.Ser1437Cys
XM_017009228.2:c.4157C>G	XP_016864717.1:p.Ser1386Cys
NM_001999.4:c.4310C>G MANE Select	NP_001990.2:p.Ser1437Cys