Canonical Allele Identifier: CA360755250
Gene: FBN2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128332998T>C , CM000667.2:g.128332998T>C GRCh38
NC_000005.9:g.127668690T>C , CM000667.1:g.127668690T>C GRCh37
NC_000005.8:g.127696589T>C NCBI36
NG_008750.1:g.210046A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000703783.1:n.920A>G
ENST00000703785.1:n.1001A>G
ENST00000262464.9:c.4136A>G MANE Select ENSP00000262464.4:p.Asp1379Gly
ENST00000262464.8:c.4136A>G ENSP00000262464.4:p.Asp1379Gly
ENST00000507835.5:c.686A>G ENSP00000426839.1:p.Asp229Gly
ENST00000508053.5:c.4136A>G ENSP00000424571.1:p.Asp1379Gly
ENST00000508989.5:c.4037A>G ENSP00000425596.1:p.Asp1346Gly
ENST00000619499.4:c.4133A>G ENSP00000482132.1:p.Asp1378Gly
NM_001999.3:c.4136A>G NP_001990.2:p.Asp1379Gly
XM_017009228.2:c.3983A>G XP_016864717.1:p.Asp1328Gly
NM_001999.4:c.4136A>G MANE Select NP_001990.2:p.Asp1379Gly