Canonical Allele Identifier: CA360757295
Community Standard Title: NM_001999.4(FBN2):c.3967T>G (p.Cys1323Gly)
Gene: FBN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128335176A>C , CM000667.2:g.128335176A>C GRCh38
NC_000005.9:g.127670868A>C , CM000667.1:g.127670868A>C GRCh37
NC_000005.8:g.127698767A>C NCBI36
NG_008750.1:g.207868T>G

Transcript Alleles

HGVS Amino-acid Change
NM_001999.4:c.3967T>G MANE Select NP_001990.2:p.Cys1323Gly
ENST00000262464.9:c.3967T>G MANE Select ENSP00000262464.4:p.Cys1323Gly
NM_001999.3:c.3967T>G NP_001990.2:p.Cys1323Gly
ENST00000262464.8:c.3967T>G ENSP00000262464.4:p.Cys1323Gly
ENST00000507835.5:c.517T>G ENSP00000426839.1:p.Cys173Gly
ENST00000508053.5:c.3967T>G ENSP00000424571.1:p.Cys1323Gly
ENST00000508989.5:c.3868T>G ENSP00000425596.1:p.Cys1290Gly
ENST00000619499.4:c.3964T>G ENSP00000482132.1:p.Cys1322Gly
ENST00000703783.1:n.751T>G
ENST00000703785.1:n.832T>G
XM_017009228.2:c.3814T>G XP_016864717.1:p.Cys1272Gly