Canonical Allele Identifier: CA360755230
Gene: FBN2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128332996T>C , CM000667.2:g.128332996T>C GRCh38
NC_000005.9:g.127668688T>C , CM000667.1:g.127668688T>C GRCh37
NC_000005.8:g.127696587T>C NCBI36
NG_008750.1:g.210048A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000703783.1:n.922A>G
ENST00000703785.1:n.1003A>G
ENST00000262464.9:c.4138A>G MANE Select ENSP00000262464.4:p.Met1380Val
ENST00000262464.8:c.4138A>G ENSP00000262464.4:p.Met1380Val
ENST00000507835.5:c.688A>G ENSP00000426839.1:p.Met230Val
ENST00000508053.5:c.4138A>G ENSP00000424571.1:p.Met1380Val
ENST00000508989.5:c.4039A>G ENSP00000425596.1:p.Met1347Val
ENST00000619499.4:c.4135A>G ENSP00000482132.1:p.Met1379Val
NM_001999.3:c.4138A>G NP_001990.2:p.Met1380Val
XM_017009228.2:c.3985A>G XP_016864717.1:p.Met1329Val
NM_001999.4:c.4138A>G MANE Select NP_001990.2:p.Met1380Val