Canonical Allele Identifier: CA360739679
Gene: FBN2 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000703783.1:n.2584G>A
ENST00000703785.1:n.2503G>A
ENST00000262464.9:c.5800G>A MANE Select ENSP00000262464.4:p.Asp1934Asn
ENST00000262464.8:c.5800G>A ENSP00000262464.4:p.Asp1934Asn
ENST00000508053.5:c.5800G>A ENSP00000424571.1:p.Asp1934Asn
ENST00000619499.4:c.5797G>A ENSP00000482132.1:p.Asp1933Asn
NM_001999.3:c.5800G>A NP_001990.2:p.Asp1934Asn
XM_017009228.2:c.5647G>A XP_016864717.1:p.Asp1883Asn
NM_001999.4:c.5800G>A MANE Select NP_001990.2:p.Asp1934Asn