Canonical Allele Identifier: CA360739703
Gene: FBN2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128304961G>C , CM000667.2:g.128304961G>C GRCh38
NC_000005.9:g.127640653G>C , CM000667.1:g.127640653G>C GRCh37
NC_000005.8:g.127668552G>C NCBI36
NG_008750.1:g.238083C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000703783.1:n.2580C>G
ENST00000703785.1:n.2499C>G
ENST00000262464.9:c.5796C>G MANE Select ENSP00000262464.4:p.Cys1932Trp
ENST00000262464.8:c.5796C>G ENSP00000262464.4:p.Cys1932Trp
ENST00000508053.5:c.5796C>G ENSP00000424571.1:p.Cys1932Trp
ENST00000619499.4:c.5793C>G ENSP00000482132.1:p.Cys1931Trp
NM_001999.3:c.5796C>G NP_001990.2:p.Cys1932Trp
XM_017009228.2:c.5643C>G XP_016864717.1:p.Cys1881Trp
NM_001999.4:c.5796C>G MANE Select NP_001990.2:p.Cys1932Trp