Canonical Allele Identifier: CA360757553

Gene: FBN2

Linked Data

• MyVariant Identifiers: chr5:g.127670970T>C (hg19) ; chr5:g.128335278T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128335278T>C , CM000667.2:g.128335278T>C	GRCh38
NC_000005.9:g.127670970T>C , CM000667.1:g.127670970T>C	GRCh37
NC_000005.8:g.127698869T>C	NCBI36
NG_008750.1:g.207766A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000703783.1:n.649A>G
ENST00000703785.1:n.730A>G
ENST00000262464.9:c.3865A>G MANE Select	ENSP00000262464.4:p.Asn1289Asp
ENST00000262464.8:c.3865A>G	ENSP00000262464.4:p.Asn1289Asp
ENST00000507835.5:c.415A>G	ENSP00000426839.1:p.Asn139Asp
ENST00000508053.5:c.3865A>G	ENSP00000424571.1:p.Asn1289Asp
ENST00000508989.5:c.3766A>G	ENSP00000425596.1:p.Asn1256Asp
ENST00000619499.4:c.3862A>G	ENSP00000482132.1:p.Asn1288Asp
NM_001999.3:c.3865A>G	NP_001990.2:p.Asn1289Asp
XM_017009228.2:c.3712A>G	XP_016864717.1:p.Asn1238Asp
NM_001999.4:c.3865A>G MANE Select	NP_001990.2:p.Asn1289Asp