Canonical Allele Identifier: CA2299446

Gene: GLB1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.33018562C>A , CM000665.2:g.33018562C>A	GRCh38
NC_000003.11:g.33060054C>A , CM000665.1:g.33060054C>A	GRCh37
NC_000003.10:g.33035058C>A	NCBI36
NG_009005.1:g.83641G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000404.4:c.1234-1G>T MANE Select	NP_000395.3:n.1234-1G>T
ENST00000307363.10:c.1234-1G>T MANE Select	ENSP00000306920.4:n.1234-1G>T
NM_000404.2:c.1234-1G>T	NP_000395.2:n.1234-1G>T
NM_000404.3:c.1234-1G>T	NP_000395.2:n.1234-1G>T
NM_001079811.1:c.1144-1G>T	NP_001073279.1:n.1144-1G>T
NM_001079811.2:c.1144-1G>T	NP_001073279.1:n.1144-1G>T
NM_001079811.3:c.1144-1G>T	NP_001073279.2:n.1144-1G>T
NM_001135602.1:c.841-1G>T	NP_001129074.1:n.841-1G>T
NM_001135602.2:c.841-1G>T	NP_001129074.1:n.841-1G>T
NM_001135602.3:c.841-1G>T	NP_001129074.2:n.841-1G>T
NM_001317040.1:c.1378-1G>T	NP_001303969.1:n.1378-1G>T
NM_001317040.2:c.1378-1G>T	NP_001303969.2:n.1378-1G>T
NM_001393580.1:c.1234-1G>T	NP_001380509.1:n.1234-1G>T
ENST00000307363.9:c.1234-1G>T	ENSP00000306920.4:n.1234-1G>T
ENST00000307377.12:c.841-1G>T	ENSP00000305920.8:n.841-1G>T
ENST00000399402.7:c.1144-1G>T	ENSP00000382333.2:n.1144-1G>T
ENST00000461475.5:n.333-1G>T
ENST00000467571.5:n.271-1G>T
ENST00000497796.5:n.486-1G>T