Canonical Allele Identifier: CA446310154

Gene: FBN2

Linked Data

• MyVariant Identifiers: chr5:g.127671217A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128335525A>G , CM000667.2:g.128335525A>G	GRCh38
NC_000005.9:g.127671217A>G , CM000667.1:g.127671217A>G	GRCh37
NC_000005.8:g.127699116A>G	NCBI36
NG_008750.1:g.207519T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703783.1:n.561T>C
ENST00000703785.1:n.642T>C
ENST00000262464.9:c.3777T>C MANE Select	ENSP00000262464.4:p.Asn1259=
ENST00000262464.8:c.3777T>C	ENSP00000262464.4:p.Asn1259=
ENST00000507835.5:c.327T>C	ENSP00000426839.1:p.Asn109=
ENST00000508053.5:c.3777T>C	ENSP00000424571.1:p.Asn1259=
ENST00000508989.5:c.3678T>C	ENSP00000425596.1:p.Asn1226=
ENST00000619499.4:c.3774T>C	ENSP00000482132.1:p.Asn1258=
NM_001999.3:c.3777T>C	NP_001990.2:p.Asn1259=
XM_017009228.2:c.3624T>C	XP_016864717.1:p.Asn1208=
NM_001999.4:c.3777T>C MANE Select	NP_001990.2:p.Asn1259=