Canonical Allele Identifier: CA803627003

Gene: FBN2

Linked Data

• dbSNP Id: rs1465092019
• gnomAD v3: 5-128301232-T-C
• gnomAD v4: 5-128301232-T-C
• MyVariant Identifiers: chr5:g.127636924T>C (hg19) ; chr5:g.128301232T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128301232T>C , CM000667.2:g.128301232T>C	GRCh38
NC_000005.9:g.127636924T>C , CM000667.1:g.127636924T>C	GRCh37
NC_000005.8:g.127664823T>C	NCBI36
NG_008750.1:g.241812A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703783.1:n.2830+150A>G
ENST00000703785.1:n.2749+150A>G
ENST00000262464.9:c.6046+150A>G MANE Select	ENSP00000262464.4:n.6046+150A>G
ENST00000262464.8:c.6046+150A>G	ENSP00000262464.4:n.6046+150A>G
ENST00000508053.5:c.6046+150A>G	ENSP00000424571.1:n.6046+150A>G
ENST00000619499.4:c.6043+150A>G	ENSP00000482132.1:n.6043+150A>G
NM_001999.3:c.6046+150A>G	NP_001990.2:n.6046+150A>G
XM_017009228.2:c.5893+150A>G	XP_016864717.1:n.5893+150A>G
NM_001999.4:c.6046+150A>G MANE Select	NP_001990.2:n.6046+150A>G