Canonical Allele Identifier: CA360759921

Gene: FBN2

Linked Data

• MyVariant Identifiers: chr5:g.127674673A>T (hg19) ; chr5:g.128338981A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128338981A>T , CM000667.2:g.128338981A>T	GRCh38
NC_000005.9:g.127674673A>T , CM000667.1:g.127674673A>T	GRCh37
NC_000005.8:g.127702572A>T	NCBI36
NG_008750.1:g.204063T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000703783.1:n.208T>A
ENST00000703785.1:n.289T>A
ENST00000262464.9:c.3424T>A MANE Select	ENSP00000262464.4:p.Cys1142Ser
ENST00000262464.8:c.3424T>A	ENSP00000262464.4:p.Cys1142Ser
ENST00000507835.5:c.-27T>A	ENSP00000426839.1:n.-27T>A
ENST00000508053.5:c.3424T>A	ENSP00000424571.1:p.Cys1142Ser
ENST00000508989.5:c.3325T>A	ENSP00000425596.1:p.Cys1109Ser
ENST00000619499.4:c.3421T>A	ENSP00000482132.1:p.Cys1141Ser
NM_001999.3:c.3424T>A	NP_001990.2:p.Cys1142Ser
XM_017009228.2:c.3271T>A	XP_016864717.1:p.Cys1091Ser
NM_001999.4:c.3424T>A MANE Select	NP_001990.2:p.Cys1142Ser