Canonical Allele Identifier: CA360753820

Gene: FBN2

Linked Data

• MyVariant Identifiers: chr5:g.127666273G>C (hg19) ; chr5:g.128330581G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128330581G>C , CM000667.2:g.128330581G>C	GRCh38
NC_000005.9:g.127666273G>C , CM000667.1:g.127666273G>C	GRCh37
NC_000005.8:g.127694172G>C	NCBI36
NG_008750.1:g.212463C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703783.1:n.1121C>G
ENST00000703785.1:n.1202C>G
ENST00000262464.9:c.4337C>G MANE Select	ENSP00000262464.4:p.Thr1446Ser
ENST00000262464.8:c.4337C>G	ENSP00000262464.4:p.Thr1446Ser
ENST00000507835.5:c.887C>G	ENSP00000426839.1:p.Thr296Ser
ENST00000508053.5:c.4337C>G	ENSP00000424571.1:p.Thr1446Ser
ENST00000508989.5:c.4238C>G	ENSP00000425596.1:p.Thr1413Ser
ENST00000619499.4:c.4334C>G	ENSP00000482132.1:p.Thr1445Ser
NM_001999.3:c.4337C>G	NP_001990.2:p.Thr1446Ser
XM_017009228.2:c.4184C>G	XP_016864717.1:p.Thr1395Ser
NM_001999.4:c.4337C>G MANE Select	NP_001990.2:p.Thr1446Ser