Canonical Allele Identifier: CA446309285
Gene: FBN2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.127636600G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128300908G>T , CM000667.2:g.128300908G>T GRCh38
NC_000005.9:g.127636600G>T , CM000667.1:g.127636600G>T GRCh37
NC_000005.8:g.127664499G>T NCBI36
NG_008750.1:g.242136C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000703783.1:n.2859C>A
ENST00000703785.1:n.2778C>A
ENST00000262464.9:c.6075C>A MANE Select ENSP00000262464.4:p.Gly2025=
ENST00000262464.8:c.6075C>A ENSP00000262464.4:p.Gly2025=
ENST00000508053.5:c.6075C>A ENSP00000424571.1:p.Gly2025=
ENST00000619499.4:c.6072C>A ENSP00000482132.1:p.Gly2024=
NM_001999.3:c.6075C>A NP_001990.2:p.Gly2025=
XM_017009228.2:c.5922C>A XP_016864717.1:p.Gly1974=
NM_001999.4:c.6075C>A MANE Select NP_001990.2:p.Gly2025=