Canonical Allele Identifier: CA360766588
Gene: FBN2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128300919C>G , CM000667.2:g.128300919C>G GRCh38
NC_000005.9:g.127636611C>G , CM000667.1:g.127636611C>G GRCh37
NC_000005.8:g.127664510C>G NCBI36
NG_008750.1:g.242125G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000703783.1:n.2848G>C
ENST00000703785.1:n.2767G>C
ENST00000262464.9:c.6064G>C MANE Select ENSP00000262464.4:p.Ala2022Pro
ENST00000262464.8:c.6064G>C ENSP00000262464.4:p.Ala2022Pro
ENST00000508053.5:c.6064G>C ENSP00000424571.1:p.Ala2022Pro
ENST00000619499.4:c.6061G>C ENSP00000482132.1:p.Ala2021Pro
NM_001999.3:c.6064G>C NP_001990.2:p.Ala2022Pro
XM_017009228.2:c.5911G>C XP_016864717.1:p.Ala1971Pro
NM_001999.4:c.6064G>C MANE Select NP_001990.2:p.Ala2022Pro