Canonical Allele Identifier: CA1581282277
Gene: FBN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128357339C= , CM000667.2:g.128357339C= GRCh38
NC_000005.9:g.127693031C= , CM000667.1:g.127693031C= GRCh37
NC_000005.8:g.127720930C= NCBI36
NG_008750.1:g.185705G=

Transcript Alleles

HGVS Amino-acid change
ENST00000262464.9:c.2611G= MANE Select ENSP00000262464.4:p.Gly871=
ENST00000262464.8:c.2611G= ENSP00000262464.4:p.Gly871=
ENST00000508053.5:c.2611G= ENSP00000424571.1:p.Gly871=
ENST00000508989.5:c.2512G= ENSP00000425596.1:p.Gly838=
ENST00000619499.4:c.2608G= ENSP00000482132.1:p.Gly870=
NM_001999.3:c.2611G= NP_001990.2:p.Gly871=
XM_017009228.2:c.2458G= XP_016864717.1:p.Gly820=
NM_001999.4:c.2611G= MANE Select NP_001990.2:p.Gly871=