Canonical Allele Identifier: CA360739695
Gene: FBN2 HGNC NCBI

Linked Data

dbSNP Id: rs1184318904

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128304959A>T , CM000667.2:g.128304959A>T GRCh38
NC_000005.9:g.127640651A>T , CM000667.1:g.127640651A>T GRCh37
NC_000005.8:g.127668550A>T NCBI36
NG_008750.1:g.238085T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000703783.1:n.2582T>A
ENST00000703785.1:n.2501T>A
ENST00000262464.9:c.5798T>A MANE Select ENSP00000262464.4:p.Met1933Lys
ENST00000262464.8:c.5798T>A ENSP00000262464.4:p.Met1933Lys
ENST00000508053.5:c.5798T>A ENSP00000424571.1:p.Met1933Lys
ENST00000619499.4:c.5795T>A ENSP00000482132.1:p.Met1932Lys
NM_001999.3:c.5798T>A NP_001990.2:p.Met1933Lys
XM_017009228.2:c.5645T>A XP_016864717.1:p.Met1882Lys
NM_001999.4:c.5798T>A MANE Select NP_001990.2:p.Met1933Lys