Canonical Allele Identifier: CA360767476
Gene: FBN2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128357366C>A , CM000667.2:g.128357366C>A GRCh38
NC_000005.9:g.127693058C>A , CM000667.1:g.127693058C>A GRCh37
NC_000005.8:g.127720957C>A NCBI36
NG_008750.1:g.185678G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262464.9:c.2584G>T MANE Select ENSP00000262464.4:p.Val862Phe
ENST00000262464.8:c.2584G>T ENSP00000262464.4:p.Val862Phe
ENST00000508053.5:c.2584G>T ENSP00000424571.1:p.Val862Phe
ENST00000508989.5:c.2485G>T ENSP00000425596.1:p.Val829Phe
ENST00000619499.4:c.2581G>T ENSP00000482132.1:p.Val861Phe
NM_001999.3:c.2584G>T NP_001990.2:p.Val862Phe
XM_017009228.2:c.2431G>T XP_016864717.1:p.Val811Phe
NM_001999.4:c.2584G>T MANE Select NP_001990.2:p.Val862Phe