Allele Registry

WARNING - Protein Allele ID and Protein Sequence HGVS API Requests Temporarily Disabled:
We are investigating the periodic unresponsiveness in the Registry.
Although replication attempts were unsuccessful, there is a high correlation with protein alleles. And with haplotype HGVS queries.
This temporarily affects the API and the UI.

ClinGen Allele Registry

Canonical Allele Identifier: CA16607112

Gene: FBN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 388980

ClinVar RCV Id: RCV000441111

dbSNP Id: rs25388

MyVariant Identifiers: chr15:g.48902965G>T (hg19) chr15:g.48610768G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48610768G>T , CM000677.2:g.48610768G>T	GRCh38
NC_000015.9:g.48902965G>T , CM000677.1:g.48902965G>T	GRCh37
NC_000015.8:g.46690257G>T	NCBI36
NG_008805.2:g.40021C>A , LRG_778:g.40021C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000559133.6:c.306C>A	ENSP00000453958.2:p.Cys102Ter
ENST00000674301.2:c.306C>A	ENSP00000501333.2:p.Cys102Ter
ENST00000316623.10:c.306C>A MANE Select	ENSP00000325527.5:p.Cys102Ter
ENST00000316623.9:c.306C>A	ENSP00000325527.5:p.Cys102Ter
ENST00000537463.6:c.306C>A	ENSP00000440294.2:p.Cys102Ter
NM_000138.4:c.306C>A , LRG_778t1:c.306C>A	NP_000129.3:p.Cys102Ter
NM_000138.5:c.306C>A MANE Select	NP_000129.3:p.Cys102Ter