Canonical Allele Identifier: CA390385003

Gene: LTBP2

Linked Data

• MyVariant Identifiers: chr14:g.74970190T>G (hg19) ; chr14:g.74503487T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.74503487T>G , CM000676.2:g.74503487T>G	GRCh38
NC_000014.8:g.74970190T>G , CM000676.1:g.74970190T>G	GRCh37
NC_000014.7:g.74039943T>G	NCBI36
NG_021486.1:g.113845A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261978.9:c.4702A>C MANE Select	ENSP00000261978.4:p.Asn1568His
ENST00000261978.8:c.4702A>C	ENSP00000261978.4:p.Asn1568His
ENST00000553939.5:c.4702A>C	ENSP00000452110.1:p.Asn1568His
ENST00000556690.5:c.4570A>C	ENSP00000451477.1:p.Asn1524His
NM_000428.2:c.4702A>C	NP_000419.1:p.Asn1568His
XM_011536765.1:c.4321A>C	XP_011535067.1:p.Asn1441His
XM_011536766.1:c.4243A>C	XP_011535068.1:p.Asn1415His
XM_011536767.1:c.4219A>C	XP_011535069.1:p.Asn1407His
XM_011536765.2:c.4321A>C	XP_011535067.1:p.Asn1441His
NM_000428.3:c.4702A>C MANE Select	NP_000419.1:p.Asn1568His