Canonical Allele Identifier: CA390398890

Gene: LTBP2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.74551266C>G , CM000676.2:g.74551266C>G	GRCh38
NC_000014.8:g.75017969C>G , CM000676.1:g.75017969C>G	GRCh37
NC_000014.7:g.74087722C>G	NCBI36
NG_021486.1:g.66066G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261978.9:c.1484G>C MANE Select	ENSP00000261978.4:p.Arg495Pro
ENST00000261978.8:c.1484G>C	ENSP00000261978.4:p.Arg495Pro
ENST00000553939.5:c.1484G>C	ENSP00000452110.1:p.Arg495Pro
ENST00000556690.5:c.1484G>C	ENSP00000451477.1:p.Arg495Pro
ENST00000557425.1:n.208G>C
NM_000428.2:c.1484G>C	NP_000419.1:p.Arg495Pro
XM_011536765.1:c.1484G>C	XP_011535067.1:p.Arg495Pro
XM_011536766.1:c.1025G>C	XP_011535068.1:p.Arg342Pro
XM_011536767.1:c.1001G>C	XP_011535069.1:p.Arg334Pro
XM_011536765.2:c.1484G>C	XP_011535067.1:p.Arg495Pro
NM_000428.3:c.1484G>C MANE Select	NP_000419.1:p.Arg495Pro