Canonical Allele Identifier: CA270013669
Gene: FBN1 HGNC NCBI

Linked Data

dbSNP Id: rs907361161
gnomAD v3: 15-48537930-A-C
gnomAD v4: 15-48537930-A-C
MyVariant Identifiers: chr15:g.48830127A>C (hg19) chr15:g.48537930A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48537930A>C , CM000677.2:g.48537930A>C GRCh38
NC_000015.9:g.48830127A>C , CM000677.1:g.48830127A>C GRCh37
NC_000015.8:g.46617419A>C NCBI36
NG_008805.2:g.112859T>G , LRG_778:g.112859T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.539-122T>G ENSP00000453958.2:n.539-122T>G
ENST00000674301.2:c.539-122T>G ENSP00000501333.2:n.539-122T>G
ENST00000316623.10:c.539-122T>G MANE Select ENSP00000325527.5:n.539-122T>G
ENST00000316623.9:c.539-122T>G ENSP00000325527.5:n.539-122T>G
ENST00000537463.6:c.539-122T>G ENSP00000440294.2:n.539-122T>G
NM_000138.4:c.539-122T>G , LRG_778t1:c.539-122T>G NP_000129.3:n.539-122T>G
NM_000138.5:c.539-122T>G MANE Select NP_000129.3:n.539-122T>G
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