Canonical Allele Identifier: CA2265374
Gene: FBLN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.13571436A>G , CM000665.2:g.13571436A>G GRCh38
NC_000003.11:g.13612936A>G , CM000665.1:g.13612936A>G GRCh37
NC_000003.10:g.13587937A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000404922.8:c.1081A>G MANE Select ENSP00000384169.3:p.Ser361Gly
ENST00000295760.11:c.1081A>G ENSP00000295760.7:p.Ser361Gly
ENST00000404922.7:c.1081A>G ENSP00000384169.3:p.Ser361Gly
ENST00000492059.5:c.1081A>G ENSP00000420042.1:p.Ser361Gly
NM_001004019.1:c.1081A>G NP_001004019.1:p.Ser361Gly
NM_001165035.1:c.1081A>G NP_001158507.1:p.Ser361Gly
NM_001998.2:c.1081A>G NP_001989.2:p.Ser361Gly
XM_006713026.2:c.1081A>G XP_006713089.1:p.Ser361Gly
NM_001004019.2:c.1081A>G MANE Select NP_001004019.1:p.Ser361Gly
NM_001165035.2:c.1081A>G NP_001158507.1:p.Ser361Gly
NM_001998.3:c.1081A>G NP_001989.2:p.Ser361Gly