Canonical Allele Identifier: CA360755224

Gene: FBN2

Linked Data

• MyVariant Identifiers: chr5:g.127668687A>G (hg19) ; chr5:g.128332995A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128332995A>G , CM000667.2:g.128332995A>G	GRCh38
NC_000005.9:g.127668687A>G , CM000667.1:g.127668687A>G	GRCh37
NC_000005.8:g.127696586A>G	NCBI36
NG_008750.1:g.210049T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000703783.1:n.923T>C
ENST00000703785.1:n.1004T>C
ENST00000262464.9:c.4139T>C MANE Select	ENSP00000262464.4:p.Met1380Thr
ENST00000262464.8:c.4139T>C	ENSP00000262464.4:p.Met1380Thr
ENST00000507835.5:c.689T>C	ENSP00000426839.1:p.Met230Thr
ENST00000508053.5:c.4139T>C	ENSP00000424571.1:p.Met1380Thr
ENST00000508989.5:c.4040T>C	ENSP00000425596.1:p.Met1347Thr
ENST00000619499.4:c.4136T>C	ENSP00000482132.1:p.Met1379Thr
NM_001999.3:c.4139T>C	NP_001990.2:p.Met1380Thr
XM_017009228.2:c.3986T>C	XP_016864717.1:p.Met1329Thr
NM_001999.4:c.4139T>C MANE Select	NP_001990.2:p.Met1380Thr