Canonical Allele Identifier: CA2628347452

Gene: FBN1

Linked Data

• gnomAD v4: 15-48444389-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48444389G>A , CM000677.2:g.48444389G>A	GRCh38
NC_000015.9:g.48736586G>A , CM000677.1:g.48736586G>A	GRCh37
NC_000015.8:g.46523878G>A	NCBI36
NG_008805.2:g.206400C>T , LRG_778:g.206400C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.6037+152C>T	ENSP00000453958.2:n.6037+152C>T
ENST00000674301.2:c.6037+152C>T	ENSP00000501333.2:n.6037+152C>T
ENST00000684448.1:n.4863C>T
ENST00000316623.10:c.6037+152C>T MANE Select	ENSP00000325527.5:n.6037+152C>T
ENST00000674301.1:c.1036+152C>T	ENSP00000501333.1:n.1036+152C>T
ENST00000316623.9:c.6037+152C>T	ENSP00000325527.5:n.6037+152C>T
ENST00000537463.6:c.*1800+152C>T	ENSP00000440294.2:n.*1800+152C>T
ENST00000559133.5:c.1344+152C>T
ENST00000560820.1:n.157+152C>T
NM_000138.4:c.6037+152C>T , LRG_778t1:c.6037+152C>T	NP_000129.3:n.6037+152C>T
NM_000138.5:c.6037+152C>T MANE Select	NP_000129.3:n.6037+152C>T