Canonical Allele Identifier: CA390382067

Gene: LTBP2

Linked Data

• MyVariant Identifiers: chr14:g.74967685G>C (hg19) ; chr14:g.74500982G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.74500982G>C , CM000676.2:g.74500982G>C	GRCh38
NC_000014.8:g.74967685G>C , CM000676.1:g.74967685G>C	GRCh37
NC_000014.7:g.74037438G>C	NCBI36
NG_021486.1:g.116350C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000261978.9:c.5368C>G MANE Select	ENSP00000261978.4:p.His1790Asp
ENST00000261978.8:c.5368C>G	ENSP00000261978.4:p.His1790Asp
ENST00000553939.5:c.*147C>G	ENSP00000452110.1:n.*147C>G
ENST00000554861.1:n.586C>G
ENST00000556690.5:c.5236C>G	ENSP00000451477.1:p.His1746Asp
NM_000428.2:c.5368C>G	NP_000419.1:p.His1790Asp
XM_011536765.1:c.4987C>G	XP_011535067.1:p.His1663Asp
XM_011536766.1:c.4909C>G	XP_011535068.1:p.His1637Asp
XM_011536767.1:c.4885C>G	XP_011535069.1:p.His1629Asp
XM_011536765.2:c.4987C>G	XP_011535067.1:p.His1663Asp
NM_000428.3:c.5368C>G MANE Select	NP_000419.1:p.His1790Asp