Canonical Allele Identifier: CA1081366555
Gene: FBN2 HGNC NCBI

Linked Data

dbSNP Id: rs1751519867
gnomAD v3: 5-128357085-A-G
gnomAD v4: 5-128357085-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128357085A>G , CM000667.2:g.128357085A>G GRCh38
NC_000005.9:g.127692777A>G , CM000667.1:g.127692777A>G GRCh37
NC_000005.8:g.127720676A>G NCBI36
NG_008750.1:g.185959T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262464.9:c.2674+191T>C MANE Select ENSP00000262464.4:n.2674+191T>C
ENST00000262464.8:c.2674+191T>C ENSP00000262464.4:n.2674+191T>C
ENST00000508053.5:c.2674+191T>C ENSP00000424571.1:n.2674+191T>C
ENST00000508989.5:c.2575+191T>C ENSP00000425596.1:n.2575+191T>C
ENST00000619499.4:c.2671+191T>C ENSP00000482132.1:n.2671+191T>C
NM_001999.3:c.2674+191T>C NP_001990.2:n.2674+191T>C
XM_017009228.2:c.2521+191T>C XP_016864717.1:n.2521+191T>C
NM_001999.4:c.2674+191T>C MANE Select NP_001990.2:n.2674+191T>C
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