Canonical Allele Identifier: CA360767400
Gene: FBN2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128357332A>C , CM000667.2:g.128357332A>C GRCh38
NC_000005.9:g.127693024A>C , CM000667.1:g.127693024A>C GRCh37
NC_000005.8:g.127720923A>C NCBI36
NG_008750.1:g.185712T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000262464.9:c.2618T>G MANE Select ENSP00000262464.4:p.Phe873Cys
ENST00000262464.8:c.2618T>G ENSP00000262464.4:p.Phe873Cys
ENST00000508053.5:c.2618T>G ENSP00000424571.1:p.Phe873Cys
ENST00000508989.5:c.2519T>G ENSP00000425596.1:p.Phe840Cys
ENST00000619499.4:c.2615T>G ENSP00000482132.1:p.Phe872Cys
NM_001999.3:c.2618T>G NP_001990.2:p.Phe873Cys
XM_017009228.2:c.2465T>G XP_016864717.1:p.Phe822Cys
NM_001999.4:c.2618T>G MANE Select NP_001990.2:p.Phe873Cys