Canonical Allele Identifier: CA2175492132

Gene: FBN1

Linked Data

• dbSNP Id: rs2043149662

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48445341C>G , CM000677.2:g.48445341C>G	GRCh38
NC_000015.9:g.48737538C>G , CM000677.1:g.48737538C>G	GRCh37
NC_000015.8:g.46524830C>G	NCBI36
NG_008805.2:g.205448G>C , LRG_778:g.205448G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.5917+35G>C	ENSP00000453958.2:n.5917+35G>C
ENST00000674301.2:c.5917+35G>C	ENSP00000501333.2:n.5917+35G>C
ENST00000684448.1:n.4591+35G>C
ENST00000316623.10:c.5917+35G>C MANE Select	ENSP00000325527.5:n.5917+35G>C
ENST00000674301.1:c.916+35G>C	ENSP00000501333.1:n.916+35G>C
ENST00000316623.9:c.5917+35G>C	ENSP00000325527.5:n.5917+35G>C
ENST00000537463.6:c.*1680+35G>C	ENSP00000440294.2:n.*1680+35G>C
ENST00000559133.5:c.1224+35G>C
ENST00000560820.1:n.37+35G>C
NM_000138.4:c.5917+35G>C , LRG_778t1:c.5917+35G>C	NP_000129.3:n.5917+35G>C
NM_000138.5:c.5917+35G>C MANE Select	NP_000129.3:n.5917+35G>C