Canonical Allele Identifier: CA1581282297
Gene: FBN2 HGNC NCBI

Linked Data

dbSNP Id: rs773419851
gnomAD v4: 5-128357415-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128357415G>T , CM000667.2:g.128357415G>T GRCh38
NC_000005.9:g.127693107G>T , CM000667.1:g.127693107G>T GRCh37
NC_000005.8:g.127721006G>T NCBI36
NG_008750.1:g.185629C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000262464.9:c.2555-20C>A MANE Select ENSP00000262464.4:n.2555-20C>A
ENST00000262464.8:c.2555-20C>A ENSP00000262464.4:n.2555-20C>A
ENST00000508053.5:c.2555-20C>A ENSP00000424571.1:n.2555-20C>A
ENST00000508989.5:c.2456-20C>A ENSP00000425596.1:n.2456-20C>A
ENST00000619499.4:c.2552-20C>A ENSP00000482132.1:n.2552-20C>A
NM_001999.3:c.2555-20C>A NP_001990.2:n.2555-20C>A
XM_017009228.2:c.2402-20C>A XP_016864717.1:n.2402-20C>A
NM_001999.4:c.2555-20C>A MANE Select NP_001990.2:n.2555-20C>A
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