Canonical Allele Identifier: CA2675120506
Gene: FBN2 HGNC NCBI

Linked Data

gnomAD v4: 5-128393077-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128393077A>T , CM000667.2:g.128393077A>T GRCh38
NC_000005.9:g.127728770A>T , CM000667.1:g.127728770A>T GRCh37
NC_000005.8:g.127756669A>T NCBI36
NG_008750.1:g.149966T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000703787.1:n.1172+58T>A
ENST00000262464.9:c.1465+58T>A MANE Select ENSP00000262464.4:n.1465+58T>A
ENST00000262464.8:c.1465+58T>A ENSP00000262464.4:n.1465+58T>A
ENST00000508053.5:c.1465+58T>A ENSP00000424571.1:n.1465+58T>A
ENST00000508989.5:c.1366+58T>A ENSP00000425596.1:n.1366+58T>A
ENST00000619499.4:c.1462+58T>A ENSP00000482132.1:n.1462+58T>A
NM_001999.3:c.1465+58T>A NP_001990.2:n.1465+58T>A
XM_017009228.2:c.1312+58T>A XP_016864717.1:n.1312+58T>A
NM_001999.4:c.1465+58T>A MANE Select NP_001990.2:n.1465+58T>A
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