Canonical Allele Identifier: CA1581255383
Gene: FBN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128304965A= , CM000667.2:g.128304965A= GRCh38
NC_000005.9:g.127640657A= , CM000667.1:g.127640657A= GRCh37
NC_000005.8:g.127668556A= NCBI36
NG_008750.1:g.238079T=

Transcript Alleles

HGVS Amino-acid change
ENST00000703783.1:n.2576T=
ENST00000703785.1:n.2495T=
ENST00000262464.9:c.5792T= MANE Select ENSP00000262464.4:p.Met1931=
ENST00000262464.8:c.5792T= ENSP00000262464.4:p.Met1931=
ENST00000508053.5:c.5792T= ENSP00000424571.1:p.Met1931=
ENST00000619499.4:c.5789T= ENSP00000482132.1:p.Met1930=
NM_001999.3:c.5792T= NP_001990.2:p.Met1931=
XM_017009228.2:c.5639T= XP_016864717.1:p.Met1880=
NM_001999.4:c.5792T= MANE Select NP_001990.2:p.Met1931=