Canonical Allele Identifier: CA390384832

Gene: LTBP2

Linked Data

• MyVariant Identifiers: chr14:g.74970060C>G (hg19) ; chr14:g.74503357C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.74503357C>G , CM000676.2:g.74503357C>G	GRCh38
NC_000014.8:g.74970060C>G , CM000676.1:g.74970060C>G	GRCh37
NC_000014.7:g.74039813C>G	NCBI36
NG_021486.1:g.113975G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261978.9:c.4750G>C MANE Select	ENSP00000261978.4:p.Asp1584His
ENST00000261978.8:c.4750G>C	ENSP00000261978.4:p.Asp1584His
ENST00000553939.5:c.4750G>C	ENSP00000452110.1:p.Asp1584His
ENST00000556690.5:c.4618G>C	ENSP00000451477.1:p.Asp1540His
NM_000428.2:c.4750G>C	NP_000419.1:p.Asp1584His
XM_011536765.1:c.4369G>C	XP_011535067.1:p.Asp1457His
XM_011536766.1:c.4291G>C	XP_011535068.1:p.Asp1431His
XM_011536767.1:c.4267G>C	XP_011535069.1:p.Asp1423His
XM_011536765.2:c.4369G>C	XP_011535067.1:p.Asp1457His
NM_000428.3:c.4750G>C MANE Select	NP_000419.1:p.Asp1584His