Canonical Allele Identifier: CA3395257

Gene: FBN2

Linked Data

• dbSNP Id: rs756660367
• ExAC: 5:127674777 A / G
• gnomAD v2: 5-127674777-A-G
• gnomAD v4: 5-128339085-A-G
• MyVariant Identifiers: chr5:g.127674777A>G (hg19) ; chr5:g.128339085A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128339085A>G , CM000667.2:g.128339085A>G	GRCh38
NC_000005.9:g.127674777A>G , CM000667.1:g.127674777A>G	GRCh37
NC_000005.8:g.127702676A>G	NCBI36
NG_008750.1:g.203959T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703783.1:n.104T>C
ENST00000703785.1:n.185T>C
ENST00000262464.9:c.3344-24T>C MANE Select	ENSP00000262464.4:n.3344-24T>C
ENST00000262464.8:c.3344-24T>C	ENSP00000262464.4:n.3344-24T>C
ENST00000507835.5:c.-131T>C	ENSP00000426839.1:n.-131T>C
ENST00000508053.5:c.3344-24T>C	ENSP00000424571.1:n.3344-24T>C
ENST00000508989.5:c.3245-24T>C	ENSP00000425596.1:n.3245-24T>C
ENST00000619499.4:c.3341-24T>C	ENSP00000482132.1:n.3341-24T>C
NM_001999.3:c.3344-24T>C	NP_001990.2:n.3344-24T>C
XM_017009228.2:c.3191-24T>C	XP_016864717.1:n.3191-24T>C
NM_001999.4:c.3344-24T>C MANE Select	NP_001990.2:n.3344-24T>C