Canonical Allele Identifier: CA360759395
Gene: FBN2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128338069T>C , CM000667.2:g.128338069T>C GRCh38
NC_000005.9:g.127673761T>C , CM000667.1:g.127673761T>C GRCh37
NC_000005.8:g.127701660T>C NCBI36
NG_008750.1:g.204975A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000703783.1:n.310A>G
ENST00000703785.1:n.391A>G
ENST00000262464.9:c.3526A>G MANE Select ENSP00000262464.4:p.Asn1176Asp
ENST00000262464.8:c.3526A>G ENSP00000262464.4:p.Asn1176Asp
ENST00000507835.5:c.76A>G ENSP00000426839.1:p.Asn26Asp
ENST00000508053.5:c.3526A>G ENSP00000424571.1:p.Asn1176Asp
ENST00000508989.5:c.3427A>G ENSP00000425596.1:p.Asn1143Asp
ENST00000619499.4:c.3523A>G ENSP00000482132.1:p.Asn1175Asp
NM_001999.3:c.3526A>G NP_001990.2:p.Asn1176Asp
XM_017009228.2:c.3373A>G XP_016864717.1:p.Asn1125Asp
NM_001999.4:c.3526A>G MANE Select NP_001990.2:p.Asn1176Asp