Canonical Allele Identifier: CA360755293
Gene: FBN2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128333003G>C , CM000667.2:g.128333003G>C GRCh38
NC_000005.9:g.127668695G>C , CM000667.1:g.127668695G>C GRCh37
NC_000005.8:g.127696594G>C NCBI36
NG_008750.1:g.210041C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000703783.1:n.915C>G
ENST00000703785.1:n.996C>G
ENST00000262464.9:c.4131C>G MANE Select ENSP00000262464.4:p.Asn1377Lys
ENST00000262464.8:c.4131C>G ENSP00000262464.4:p.Asn1377Lys
ENST00000507835.5:c.681C>G ENSP00000426839.1:p.Asn227Lys
ENST00000508053.5:c.4131C>G ENSP00000424571.1:p.Asn1377Lys
ENST00000508989.5:c.4032C>G ENSP00000425596.1:p.Asn1344Lys
ENST00000619499.4:c.4128C>G ENSP00000482132.1:p.Asn1376Lys
NM_001999.3:c.4131C>G NP_001990.2:p.Asn1377Lys
XM_017009228.2:c.3978C>G XP_016864717.1:p.Asn1326Lys
NM_001999.4:c.4131C>G MANE Select NP_001990.2:p.Asn1377Lys