Canonical Allele Identifier: CA1581282274
Gene: FBN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128357330T= , CM000667.2:g.128357330T= GRCh38
NC_000005.9:g.127693022T= , CM000667.1:g.127693022T= GRCh37
NC_000005.8:g.127720921T= NCBI36
NG_008750.1:g.185714A=

Transcript Alleles

HGVS Amino-acid change
ENST00000262464.9:c.2620A= MANE Select ENSP00000262464.4:p.Asn874=
ENST00000262464.8:c.2620A= ENSP00000262464.4:p.Asn874=
ENST00000508053.5:c.2620A= ENSP00000424571.1:p.Asn874=
ENST00000508989.5:c.2521A= ENSP00000425596.1:p.Asn841=
ENST00000619499.4:c.2617A= ENSP00000482132.1:p.Asn873=
NM_001999.3:c.2620A= NP_001990.2:p.Asn874=
XM_017009228.2:c.2467A= XP_016864717.1:p.Asn823=
NM_001999.4:c.2620A= MANE Select NP_001990.2:p.Asn874=