Canonical Allele Identifier: CA360761649
Gene: FBN2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128344390C>G , CM000667.2:g.128344390C>G GRCh38
NC_000005.9:g.127680082C>G , CM000667.1:g.127680082C>G GRCh37
NC_000005.8:g.127707981C>G NCBI36
NG_008750.1:g.198654G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000262464.9:c.3338G>C MANE Select ENSP00000262464.4:p.Cys1113Ser
ENST00000262464.8:c.3338G>C ENSP00000262464.4:p.Cys1113Ser
ENST00000508053.5:c.3338G>C ENSP00000424571.1:p.Cys1113Ser
ENST00000508989.5:c.3239G>C ENSP00000425596.1:p.Cys1080Ser
ENST00000619499.4:c.3335G>C ENSP00000482132.1:p.Cys1112Ser
NM_001999.3:c.3338G>C NP_001990.2:p.Cys1113Ser
XM_017009228.2:c.3185G>C XP_016864717.1:p.Cys1062Ser
NM_001999.4:c.3338G>C MANE Select NP_001990.2:p.Cys1113Ser