Canonical Allele Identifier: CA354739613

Gene: PCCB

Linked Data

• gnomAD v4: 3-136261990-T-G
• MyVariant Identifiers: chr3:g.135980832T>G (hg19) ; chr3:g.136261990T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.136261990T>G , CM000665.2:g.136261990T>G	GRCh38
NC_000003.11:g.135980832T>G , CM000665.1:g.135980832T>G	GRCh37
NC_000003.10:g.137463522T>G	NCBI36
NG_008939.1:g.16666T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000251654.9:c.468T>G MANE Select	ENSP00000251654.4:p.Ile156Met
ENST00000251654.8:c.468T>G	ENSP00000251654.4:p.Ile156Met
ENST00000459873.1:c.219T>G	ENSP00000419293.1:p.Ile73Met
ENST00000462542.5:c.335T>G
ENST00000462637.5:c.399T>G	ENSP00000420391.1:p.Ile133Met
ENST00000465176.5:n.430T>G
ENST00000465423.5:c.555T>G	ENSP00000419263.1:p.Ile185Met
ENST00000466072.5:c.468T>G	ENSP00000420158.1:p.Ile156Met
ENST00000468777.5:c.561T>G	ENSP00000419129.1:p.Ile187Met
ENST00000469217.5:c.528T>G	ENSP00000419027.1:p.Ile176Met
ENST00000471595.5:c.468T>G	ENSP00000417549.1:p.Ile156Met
ENST00000473073.1:n.425T>G
ENST00000474833.5:n.168+11432T>G
ENST00000475214.5:n.382T>G
ENST00000478469.5:c.468T>G	ENSP00000420759.1:p.Ile156Met
ENST00000482086.5:c.120T>G	ENSP00000417253.1:p.Ile40Met
ENST00000483687.5:c.411T>G	ENSP00000420639.1:p.Ile137Met
ENST00000484181.5:c.468T>G	ENSP00000417937.1:p.Ile156Met
ENST00000490504.5:c.372+5367T>G	ENSP00000418307.1:n.372+5367T>G
ENST00000494742.5:c.219T>G	ENSP00000418020.1:p.Ile73Met
NM_000532.4:c.468T>G	NP_000523.2:p.Ile156Met
NM_001178014.1:c.528T>G	NP_001171485.1:p.Ile176Met
XM_011512873.1:c.468T>G	XP_011511175.1:p.Ile156Met
XM_011512873.2:c.468T>G	XP_011511175.1:p.Ile156Met
NM_000532.5:c.468T>G MANE Select	NP_000523.2:p.Ile156Met
NM_001178014.2:c.528T>G	NP_001171485.1:p.Ile176Met