Canonical Allele Identifier: CA2675120519
Gene: FBN2 HGNC NCBI

Linked Data

gnomAD v4: 5-128393109-A-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128393109A>G , CM000667.2:g.128393109A>G GRCh38
NC_000005.9:g.127728802A>G , CM000667.1:g.127728802A>G GRCh37
NC_000005.8:g.127756701A>G NCBI36
NG_008750.1:g.149934T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000703787.1:n.1172+26T>C
ENST00000262464.9:c.1465+26T>C MANE Select ENSP00000262464.4:n.1465+26T>C
ENST00000262464.8:c.1465+26T>C ENSP00000262464.4:n.1465+26T>C
ENST00000508053.5:c.1465+26T>C ENSP00000424571.1:n.1465+26T>C
ENST00000508989.5:c.1366+26T>C ENSP00000425596.1:n.1366+26T>C
ENST00000619499.4:c.1462+26T>C ENSP00000482132.1:n.1462+26T>C
NM_001999.3:c.1465+26T>C NP_001990.2:n.1465+26T>C
XM_017009228.2:c.1312+26T>C XP_016864717.1:n.1312+26T>C
NM_001999.4:c.1465+26T>C MANE Select NP_001990.2:n.1465+26T>C
Search 100 bp 5'
Search 100 bp 3'