Canonical Allele Identifier: CA72670746

Gene: GLB1

Linked Data

• dbSNP Id: rs926047748
• gnomAD v2: 3-33110180-A-G
• gnomAD v3: 3-33068688-A-G
• gnomAD v4: 3-33068688-A-G
• MyVariant Identifiers: chr3:g.33110180A>G (hg19) ; chr3:g.33068688A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.33068688A>G , CM000665.2:g.33068688A>G	GRCh38
NC_000003.11:g.33110180A>G , CM000665.1:g.33110180A>G	GRCh37
NC_000003.10:g.33085184A>G	NCBI36
NG_009005.1:g.33515T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307363.10:c.396+132T>C MANE Select	ENSP00000306920.4:n.396+132T>C
ENST00000307363.9:c.396+132T>C	ENSP00000306920.4:n.396+132T>C
ENST00000307377.12:c.246-3131T>C	ENSP00000305920.8:n.246-3131T>C
ENST00000399402.7:c.306+132T>C	ENSP00000382333.2:n.306+132T>C
ENST00000415454.1:c.76-10419T>C	ENSP00000411813.1:n.76-10419T>C
ENST00000438227.1:c.76-3131T>C	ENSP00000401250.1:n.76-3131T>C
ENST00000440656.1:c.3+132T>C	ENSP00000411769.1:n.3+132T>C
ENST00000446732.5:c.156-3131T>C	ENSP00000407365.1:n.156-3131T>C
ENST00000464355.1:n.354+132T>C
ENST00000482097.5:n.109-15139T>C
ENST00000485698.5:n.137-15139T>C
ENST00000498537.5:n.133-15139T>C
NM_000404.2:c.396+132T>C	NP_000395.2:n.396+132T>C
NM_000404.3:c.396+132T>C	NP_000395.2:n.396+132T>C
NM_001079811.1:c.306+132T>C	NP_001073279.1:n.306+132T>C
NM_001079811.2:c.306+132T>C	NP_001073279.1:n.306+132T>C
NM_001135602.1:c.246-3131T>C	NP_001129074.1:n.246-3131T>C
NM_001135602.2:c.246-3131T>C	NP_001129074.1:n.246-3131T>C
NM_001317040.1:c.540+132T>C	NP_001303969.1:n.540+132T>C
NM_000404.4:c.396+132T>C MANE Select	NP_000395.3:n.396+132T>C
NM_001079811.3:c.306+132T>C	NP_001073279.2:n.306+132T>C
NM_001135602.3:c.246-3131T>C	NP_001129074.2:n.246-3131T>C
NM_001317040.2:c.540+132T>C	NP_001303969.2:n.540+132T>C
NM_001393580.1:c.396+132T>C	NP_001380509.1:n.396+132T>C