Canonical Allele Identifier: CA360759920
Community Standard Title: NM_001999.4(FBN2):c.3424T>C (p.Cys1142Arg)
Gene: FBN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128338981A>G , CM000667.2:g.128338981A>G GRCh38
NC_000005.9:g.127674673A>G , CM000667.1:g.127674673A>G GRCh37
NC_000005.8:g.127702572A>G NCBI36
NG_008750.1:g.204063T>C

Transcript Alleles

HGVS Amino-acid Change
NM_001999.4:c.3424T>C MANE Select NP_001990.2:p.Cys1142Arg
ENST00000262464.9:c.3424T>C MANE Select ENSP00000262464.4:p.Cys1142Arg
NM_001999.3:c.3424T>C NP_001990.2:p.Cys1142Arg
ENST00000262464.8:c.3424T>C ENSP00000262464.4:p.Cys1142Arg
ENST00000507835.5:c.-27T>C ENSP00000426839.1:n.-27T>C
ENST00000508053.5:c.3424T>C ENSP00000424571.1:p.Cys1142Arg
ENST00000508989.5:c.3325T>C ENSP00000425596.1:p.Cys1109Arg
ENST00000619499.4:c.3421T>C ENSP00000482132.1:p.Cys1141Arg
ENST00000703783.1:n.208T>C
ENST00000703785.1:n.289T>C
XM_017009228.2:c.3271T>C XP_016864717.1:p.Cys1091Arg