Canonical Allele Identifier: CA360766573
Gene: FBN2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128300913G>C , CM000667.2:g.128300913G>C GRCh38
NC_000005.9:g.127636605G>C , CM000667.1:g.127636605G>C GRCh37
NC_000005.8:g.127664504G>C NCBI36
NG_008750.1:g.242131C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000703783.1:n.2854C>G
ENST00000703785.1:n.2773C>G
ENST00000262464.9:c.6070C>G MANE Select ENSP00000262464.4:p.Pro2024Ala
ENST00000262464.8:c.6070C>G ENSP00000262464.4:p.Pro2024Ala
ENST00000508053.5:c.6070C>G ENSP00000424571.1:p.Pro2024Ala
ENST00000619499.4:c.6067C>G ENSP00000482132.1:p.Pro2023Ala
NM_001999.3:c.6070C>G NP_001990.2:p.Pro2024Ala
XM_017009228.2:c.5917C>G XP_016864717.1:p.Pro1973Ala
NM_001999.4:c.6070C>G MANE Select NP_001990.2:p.Pro2024Ala