Canonical Allele Identifier: CA3131046685
Community Standard Title: NM_001999.4(FBN2):c.3830A= (p.Asp1277=)
Gene: FBN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128335472T= , CM000667.2:g.128335472T= GRCh38
NC_000005.9:g.127671164T= , CM000667.1:g.127671164T= GRCh37
NC_000005.8:g.127699063T= NCBI36
NG_008750.1:g.207572A=

Transcript Alleles

HGVS Amino-acid Change
NM_001999.4:c.3830A= MANE Select NP_001990.2:p.Asp1277=
ENST00000262464.9:c.3830A= MANE Select ENSP00000262464.4:p.Asp1277=
NM_001999.3:c.3830A= NP_001990.2:p.Asp1277=
ENST00000262464.8:c.3830A= ENSP00000262464.4:p.Asp1277=
ENST00000507835.5:c.380A= ENSP00000426839.1:p.Asp127=
ENST00000508053.5:c.3830A= ENSP00000424571.1:p.Asp1277=
ENST00000508989.5:c.3731A= ENSP00000425596.1:p.Asp1244=
ENST00000619499.4:c.3827A= ENSP00000482132.1:p.Asp1276=
ENST00000703783.1:n.614A=
ENST00000703785.1:n.695A=
XM_017009228.2:c.3677A= XP_016864717.1:p.Asp1226=