Canonical Allele Identifier: CA360754117

Gene: FBN2

Linked Data

• MyVariant Identifiers: chr5:g.127666343C>G (hg19) ; chr5:g.128330651C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128330651C>G , CM000667.2:g.128330651C>G	GRCh38
NC_000005.9:g.127666343C>G , CM000667.1:g.127666343C>G	GRCh37
NC_000005.8:g.127694242C>G	NCBI36
NG_008750.1:g.212393G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703783.1:n.1051G>C
ENST00000703785.1:n.1132G>C
ENST00000262464.9:c.4267G>C MANE Select	ENSP00000262464.4:p.Ala1423Pro
ENST00000262464.8:c.4267G>C	ENSP00000262464.4:p.Ala1423Pro
ENST00000507835.5:c.817G>C	ENSP00000426839.1:p.Ala273Pro
ENST00000508053.5:c.4267G>C	ENSP00000424571.1:p.Ala1423Pro
ENST00000508989.5:c.4168G>C	ENSP00000425596.1:p.Ala1390Pro
ENST00000619499.4:c.4264G>C	ENSP00000482132.1:p.Ala1422Pro
NM_001999.3:c.4267G>C	NP_001990.2:p.Ala1423Pro
XM_017009228.2:c.4114G>C	XP_016864717.1:p.Ala1372Pro
NM_001999.4:c.4267G>C MANE Select	NP_001990.2:p.Ala1423Pro