Canonical Allele Identifier: CA2147073456

Gene: LTBP2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.74500980A= , CM000676.2:g.74500980A=	GRCh38
NC_000014.8:g.74967683A= , CM000676.1:g.74967683A=	GRCh37
NC_000014.7:g.74037436A=	NCBI36
NG_021486.1:g.116352T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261978.9:c.5370T= MANE Select	ENSP00000261978.4:p.His1790=
ENST00000261978.8:c.5370T=	ENSP00000261978.4:p.His1790=
ENST00000553939.5:c.*149T=	ENSP00000452110.1:n.*149T=
ENST00000554861.1:n.588T=
ENST00000556690.5:c.5238T=	ENSP00000451477.1:p.His1746=
NM_000428.2:c.5370T=	NP_000419.1:p.His1790=
XM_011536765.1:c.4989T=	XP_011535067.1:p.His1663=
XM_011536766.1:c.4911T=	XP_011535068.1:p.His1637=
XM_011536767.1:c.4887T=	XP_011535069.1:p.His1629=
XM_011536765.2:c.4989T=	XP_011535067.1:p.His1663=
NM_000428.3:c.5370T= MANE Select	NP_000419.1:p.His1790=