Canonical Allele Identifier: CA360750611
Gene: FBN2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128395179G>C , CM000667.2:g.128395179G>C GRCh38
NC_000005.9:g.127730872G>C , CM000667.1:g.127730872G>C GRCh37
NC_000005.8:g.127758771G>C NCBI36
NG_008750.1:g.147864C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000703787.1:n.881C>G
ENST00000262464.9:c.1174C>G MANE Select ENSP00000262464.4:p.Pro392Ala
ENST00000262464.8:c.1174C>G ENSP00000262464.4:p.Pro392Ala
ENST00000508053.5:c.1174C>G ENSP00000424571.1:p.Pro392Ala
ENST00000508989.5:c.1075C>G ENSP00000425596.1:p.Pro359Ala
ENST00000619499.4:c.1171C>G ENSP00000482132.1:p.Pro391Ala
NM_001999.3:c.1174C>G NP_001990.2:p.Pro392Ala
XM_017009228.2:c.1079-1811C>G XP_016864717.1:n.1079-1811C>G
NM_001999.4:c.1174C>G MANE Select NP_001990.2:p.Pro392Ala