Canonical Allele Identifier: CA446312327

Gene: FBN2

Linked Data

• MyVariant Identifiers: chr5:g.127693023G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128357331G>A , CM000667.2:g.128357331G>A	GRCh38
NC_000005.9:g.127693023G>A , CM000667.1:g.127693023G>A	GRCh37
NC_000005.8:g.127720922G>A	NCBI36
NG_008750.1:g.185713C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262464.9:c.2619C>T MANE Select	ENSP00000262464.4:p.Phe873=
ENST00000262464.8:c.2619C>T	ENSP00000262464.4:p.Phe873=
ENST00000508053.5:c.2619C>T	ENSP00000424571.1:p.Phe873=
ENST00000508989.5:c.2520C>T	ENSP00000425596.1:p.Phe840=
ENST00000619499.4:c.2616C>T	ENSP00000482132.1:p.Phe872=
NM_001999.3:c.2619C>T	NP_001990.2:p.Phe873=
XM_017009228.2:c.2466C>T	XP_016864717.1:p.Phe822=
NM_001999.4:c.2619C>T MANE Select	NP_001990.2:p.Phe873=