Canonical Allele Identifier: CA360759447
Gene: FBN2 HGNC NCBI

Linked Data

dbSNP Id: rs1436430760

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128338083C>G , CM000667.2:g.128338083C>G GRCh38
NC_000005.9:g.127673775C>G , CM000667.1:g.127673775C>G GRCh37
NC_000005.8:g.127701674C>G NCBI36
NG_008750.1:g.204961G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000703783.1:n.296G>C
ENST00000703785.1:n.377G>C
ENST00000262464.9:c.3512G>C MANE Select ENSP00000262464.4:p.Gly1171Ala
ENST00000262464.8:c.3512G>C ENSP00000262464.4:p.Gly1171Ala
ENST00000507835.5:c.62G>C ENSP00000426839.1:p.Gly21Ala
ENST00000508053.5:c.3512G>C ENSP00000424571.1:p.Gly1171Ala
ENST00000508989.5:c.3413G>C ENSP00000425596.1:p.Gly1138Ala
ENST00000619499.4:c.3509G>C ENSP00000482132.1:p.Gly1170Ala
NM_001999.3:c.3512G>C NP_001990.2:p.Gly1171Ala
XM_017009228.2:c.3359G>C XP_016864717.1:p.Gly1120Ala
NM_001999.4:c.3512G>C MANE Select NP_001990.2:p.Gly1171Ala