Canonical Allele Identifier: CA360767407
Gene: FBN2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128357335G>C , CM000667.2:g.128357335G>C GRCh38
NC_000005.9:g.127693027G>C , CM000667.1:g.127693027G>C GRCh37
NC_000005.8:g.127720926G>C NCBI36
NG_008750.1:g.185709C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000262464.9:c.2615C>G MANE Select ENSP00000262464.4:p.Ser872Cys
ENST00000262464.8:c.2615C>G ENSP00000262464.4:p.Ser872Cys
ENST00000508053.5:c.2615C>G ENSP00000424571.1:p.Ser872Cys
ENST00000508989.5:c.2516C>G ENSP00000425596.1:p.Ser839Cys
ENST00000619499.4:c.2612C>G ENSP00000482132.1:p.Ser871Cys
NM_001999.3:c.2615C>G NP_001990.2:p.Ser872Cys
XM_017009228.2:c.2462C>G XP_016864717.1:p.Ser821Cys
NM_001999.4:c.2615C>G MANE Select NP_001990.2:p.Ser872Cys