Canonical Allele Identifier: CA360739682
Gene: FBN2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128304957C>A , CM000667.2:g.128304957C>A GRCh38
NC_000005.9:g.127640649C>A , CM000667.1:g.127640649C>A GRCh37
NC_000005.8:g.127668548C>A NCBI36
NG_008750.1:g.238087G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000703783.1:n.2584G>T
ENST00000703785.1:n.2503G>T
ENST00000262464.9:c.5800G>T MANE Select ENSP00000262464.4:p.Asp1934Tyr
ENST00000262464.8:c.5800G>T ENSP00000262464.4:p.Asp1934Tyr
ENST00000508053.5:c.5800G>T ENSP00000424571.1:p.Asp1934Tyr
ENST00000619499.4:c.5797G>T ENSP00000482132.1:p.Asp1933Tyr
NM_001999.3:c.5800G>T NP_001990.2:p.Asp1934Tyr
XM_017009228.2:c.5647G>T XP_016864717.1:p.Asp1883Tyr
NM_001999.4:c.5800G>T MANE Select NP_001990.2:p.Asp1934Tyr