Canonical Allele Identifier: CA351994440

Gene: GLB1

Linked Data

• MyVariant Identifiers: chr3:g.33110312C>A (hg19) ; chr3:g.33068820C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.33068820C>A , CM000665.2:g.33068820C>A	GRCh38
NC_000003.11:g.33110312C>A , CM000665.1:g.33110312C>A	GRCh37
NC_000003.10:g.33085316C>A	NCBI36
NG_009005.1:g.33383G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000307363.10:c.396G>T MANE Select	ENSP00000306920.4:p.Met132Ile
ENST00000307363.9:c.396G>T	ENSP00000306920.4:p.Met132Ile
ENST00000307377.12:c.246-3263G>T	ENSP00000305920.8:n.246-3263G>T
ENST00000399402.7:c.306G>T	ENSP00000382333.2:p.Met102Ile
ENST00000415454.1:c.76-10551G>T	ENSP00000411813.1:n.76-10551G>T
ENST00000438227.1:c.76-3263G>T	ENSP00000401250.1:n.76-3263G>T
ENST00000440656.1:c.3G>T	ENSP00000411769.1:p.Met1Ile
ENST00000446732.5:c.156-3263G>T	ENSP00000407365.1:n.156-3263G>T
ENST00000450835.1:c.306G>T	ENSP00000403264.1:p.Met102Ile
ENST00000464355.1:n.354G>T
ENST00000482097.5:n.109-15271G>T
ENST00000485698.5:n.137-15271G>T
ENST00000498537.5:n.133-15271G>T
NM_000404.2:c.396G>T	NP_000395.2:p.Met132Ile
NM_000404.3:c.396G>T	NP_000395.2:p.Met132Ile
NM_001079811.1:c.306G>T	NP_001073279.1:p.Met102Ile
NM_001079811.2:c.306G>T	NP_001073279.1:p.Met102Ile
NM_001135602.1:c.246-3263G>T	NP_001129074.1:n.246-3263G>T
NM_001135602.2:c.246-3263G>T	NP_001129074.1:n.246-3263G>T
NM_001317040.1:c.540G>T	NP_001303969.1:p.Met180Ile
NM_000404.4:c.396G>T MANE Select	NP_000395.3:p.Met132Ile
NM_001079811.3:c.306G>T	NP_001073279.2:p.Met102Ile
NM_001135602.3:c.246-3263G>T	NP_001129074.2:n.246-3263G>T
NM_001317040.2:c.540G>T	NP_001303969.2:p.Met180Ile
NM_001393580.1:c.396G>T	NP_001380509.1:p.Met132Ile