Canonical Allele Identifier: CA3395245
Gene: FBN2 HGNC NCBI

Linked Data

dbSNP Id: rs779345186

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128338995C>T , CM000667.2:g.128338995C>T GRCh38
NC_000005.9:g.127674687C>T , CM000667.1:g.127674687C>T GRCh37
NC_000005.8:g.127702586C>T NCBI36
NG_008750.1:g.204049G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000703783.1:n.194G>A
ENST00000703785.1:n.275G>A
ENST00000262464.9:c.3410G>A MANE Select ENSP00000262464.4:p.Ser1137Asn
ENST00000262464.8:c.3410G>A ENSP00000262464.4:p.Ser1137Asn
ENST00000507835.5:c.-41G>A ENSP00000426839.1:n.-41G>A
ENST00000508053.5:c.3410G>A ENSP00000424571.1:p.Ser1137Asn
ENST00000508989.5:c.3311G>A ENSP00000425596.1:p.Ser1104Asn
ENST00000619499.4:c.3407G>A ENSP00000482132.1:p.Ser1136Asn
NM_001999.3:c.3410G>A NP_001990.2:p.Ser1137Asn
XM_017009228.2:c.3257G>A XP_016864717.1:p.Ser1086Asn
NM_001999.4:c.3410G>A MANE Select NP_001990.2:p.Ser1137Asn