Canonical Allele Identifier: CA360755312
Gene: FBN2 HGNC NCBI

Linked Data

dbSNP Id: rs1255550274

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128333007T>A , CM000667.2:g.128333007T>A GRCh38
NC_000005.9:g.127668699T>A , CM000667.1:g.127668699T>A GRCh37
NC_000005.8:g.127696598T>A NCBI36
NG_008750.1:g.210037A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000703783.1:n.911A>T
ENST00000703785.1:n.992A>T
ENST00000262464.9:c.4127A>T MANE Select ENSP00000262464.4:p.His1376Leu
ENST00000262464.8:c.4127A>T ENSP00000262464.4:p.His1376Leu
ENST00000507835.5:c.677A>T ENSP00000426839.1:p.His226Leu
ENST00000508053.5:c.4127A>T ENSP00000424571.1:p.His1376Leu
ENST00000508989.5:c.4028A>T ENSP00000425596.1:p.His1343Leu
ENST00000619499.4:c.4124A>T ENSP00000482132.1:p.His1375Leu
NM_001999.3:c.4127A>T NP_001990.2:p.His1376Leu
XM_017009228.2:c.3974A>T XP_016864717.1:p.His1325Leu
NM_001999.4:c.4127A>T MANE Select NP_001990.2:p.His1376Leu