Canonical Allele Identifier: CA352000569

Gene: GLB1

Linked Data

• MyVariant Identifiers: chr3:g.33038724A>G (hg19) ; chr3:g.32997232A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.32997232A>G , CM000665.2:g.32997232A>G	GRCh38
NC_000003.11:g.33038724A>G , CM000665.1:g.33038724A>G	GRCh37
NC_000003.10:g.33013728A>G	NCBI36
NG_009005.1:g.104971T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307363.10:c.1847T>C MANE Select	ENSP00000306920.4:p.Ile616Thr
ENST00000307363.9:c.1847T>C	ENSP00000306920.4:p.Ile616Thr
ENST00000307377.12:c.1454T>C	ENSP00000305920.8:p.Ile485Thr
ENST00000399402.7:c.1757T>C	ENSP00000382333.2:p.Ile586Thr
NM_000404.2:c.1847T>C	NP_000395.2:p.Ile616Thr
NM_000404.3:c.1847T>C	NP_000395.2:p.Ile616Thr
NM_001079811.1:c.1757T>C	NP_001073279.1:p.Ile586Thr
NM_001079811.2:c.1757T>C	NP_001073279.1:p.Ile586Thr
NM_001135602.1:c.1454T>C	NP_001129074.1:p.Ile485Thr
NM_001135602.2:c.1454T>C	NP_001129074.1:p.Ile485Thr
NM_001317040.1:c.1991T>C	NP_001303969.1:p.Ile664Thr
NM_000404.4:c.1847T>C MANE Select	NP_000395.3:p.Ile616Thr
NM_001079811.3:c.1757T>C	NP_001073279.2:p.Ile586Thr
NM_001135602.3:c.1454T>C	NP_001129074.2:p.Ile485Thr
NM_001317040.2:c.1991T>C	NP_001303969.2:p.Ile664Thr
NM_001393580.1:c.1734+16824T>C	NP_001380509.1:n.1734+16824T>C