Canonical Allele Identifier: CA360761667
Gene: FBN2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128344394T>C , CM000667.2:g.128344394T>C GRCh38
NC_000005.9:g.127680086T>C , CM000667.1:g.127680086T>C GRCh37
NC_000005.8:g.127707985T>C NCBI36
NG_008750.1:g.198650A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000262464.9:c.3334A>G MANE Select ENSP00000262464.4:p.Asn1112Asp
ENST00000262464.8:c.3334A>G ENSP00000262464.4:p.Asn1112Asp
ENST00000508053.5:c.3334A>G ENSP00000424571.1:p.Asn1112Asp
ENST00000508989.5:c.3235A>G ENSP00000425596.1:p.Asn1079Asp
ENST00000619499.4:c.3331A>G ENSP00000482132.1:p.Asn1111Asp
NM_001999.3:c.3334A>G NP_001990.2:p.Asn1112Asp
XM_017009228.2:c.3181A>G XP_016864717.1:p.Asn1061Asp
NM_001999.4:c.3334A>G MANE Select NP_001990.2:p.Asn1112Asp