Canonical Allele Identifier: CA446310089
Gene: FBN2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.127670959A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128335267A>G , CM000667.2:g.128335267A>G GRCh38
NC_000005.9:g.127670959A>G , CM000667.1:g.127670959A>G GRCh37
NC_000005.8:g.127698858A>G NCBI36
NG_008750.1:g.207777T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000703783.1:n.660T>C
ENST00000703785.1:n.741T>C
ENST00000262464.9:c.3876T>C MANE Select ENSP00000262464.4:p.Asp1292=
ENST00000262464.8:c.3876T>C ENSP00000262464.4:p.Asp1292=
ENST00000507835.5:c.426T>C ENSP00000426839.1:p.Asp142=
ENST00000508053.5:c.3876T>C ENSP00000424571.1:p.Asp1292=
ENST00000508989.5:c.3777T>C ENSP00000425596.1:p.Asp1259=
ENST00000619499.4:c.3873T>C ENSP00000482132.1:p.Asp1291=
NM_001999.3:c.3876T>C NP_001990.2:p.Asp1292=
XM_017009228.2:c.3723T>C XP_016864717.1:p.Asp1241=
NM_001999.4:c.3876T>C MANE Select NP_001990.2:p.Asp1292=