Canonical Allele Identifier: CA360767492
Gene: FBN2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128357372G>C , CM000667.2:g.128357372G>C GRCh38
NC_000005.9:g.127693064G>C , CM000667.1:g.127693064G>C GRCh37
NC_000005.8:g.127720963G>C NCBI36
NG_008750.1:g.185672C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262464.9:c.2578C>G MANE Select ENSP00000262464.4:p.Pro860Ala
ENST00000262464.8:c.2578C>G ENSP00000262464.4:p.Pro860Ala
ENST00000508053.5:c.2578C>G ENSP00000424571.1:p.Pro860Ala
ENST00000508989.5:c.2479C>G ENSP00000425596.1:p.Pro827Ala
ENST00000619499.4:c.2575C>G ENSP00000482132.1:p.Pro859Ala
NM_001999.3:c.2578C>G NP_001990.2:p.Pro860Ala
XM_017009228.2:c.2425C>G XP_016864717.1:p.Pro809Ala
NM_001999.4:c.2578C>G MANE Select NP_001990.2:p.Pro860Ala