Canonical Allele Identifier: CA618011943
Gene: FBN1 HGNC NCBI

Linked Data

dbSNP Id: rs1177420128

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48537551G>C , CM000677.2:g.48537551G>C GRCh38
NC_000015.9:g.48829748G>C , CM000677.1:g.48829748G>C GRCh37
NC_000015.8:g.46617040G>C NCBI36
NG_008805.2:g.113238C>G , LRG_778:g.113238C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000559133.6:c.736+60C>G ENSP00000453958.2:n.736+60C>G
ENST00000674301.2:c.736+60C>G ENSP00000501333.2:n.736+60C>G
ENST00000316623.10:c.736+60C>G MANE Select ENSP00000325527.5:n.736+60C>G
ENST00000316623.9:c.736+60C>G ENSP00000325527.5:n.736+60C>G
ENST00000537463.6:c.636+160C>G ENSP00000440294.2:n.636+160C>G
NM_000138.4:c.736+60C>G , LRG_778t1:c.736+60C>G NP_000129.3:n.736+60C>G
NM_000138.5:c.736+60C>G MANE Select NP_000129.3:n.736+60C>G