Canonical Allele Identifier: CA360766173
Gene: FBN2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128300824G>T , CM000667.2:g.128300824G>T GRCh38
NC_000005.9:g.127636516G>T , CM000667.1:g.127636516G>T GRCh37
NC_000005.8:g.127664415G>T NCBI36
NG_008750.1:g.242220C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000703783.1:n.2943C>A
ENST00000703785.1:n.2862C>A
ENST00000262464.9:c.6159C>A MANE Select ENSP00000262464.4:p.Asn2053Lys
ENST00000262464.8:c.6159C>A ENSP00000262464.4:p.Asn2053Lys
ENST00000508053.5:c.6159C>A ENSP00000424571.1:p.Asn2053Lys
ENST00000619499.4:c.6156C>A ENSP00000482132.1:p.Asn2052Lys
NM_001999.3:c.6159C>A NP_001990.2:p.Asn2053Lys
XM_017009228.2:c.6006C>A XP_016864717.1:p.Asn2002Lys
NM_001999.4:c.6159C>A MANE Select NP_001990.2:p.Asn2053Lys