Canonical Allele Identifier: CA354739552

Gene: PCCB

Linked Data

• MyVariant Identifiers: chr3:g.135980809A>G (hg19) ; chr3:g.136261967A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.136261967A>G , CM000665.2:g.136261967A>G	GRCh38
NC_000003.11:g.135980809A>G , CM000665.1:g.135980809A>G	GRCh37
NC_000003.10:g.137463499A>G	NCBI36
NG_008939.1:g.16643A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251654.9:c.445A>G MANE Select	ENSP00000251654.4:p.Ile149Val
ENST00000251654.8:c.445A>G	ENSP00000251654.4:p.Ile149Val
ENST00000459873.1:c.196A>G	ENSP00000419293.1:p.Ile66Val
ENST00000462542.5:c.312A>G
ENST00000462637.5:c.376A>G	ENSP00000420391.1:p.Ile126Val
ENST00000465176.5:n.407A>G
ENST00000465423.5:c.532A>G	ENSP00000419263.1:p.Ile178Val
ENST00000466072.5:c.445A>G	ENSP00000420158.1:p.Ile149Val
ENST00000468777.5:c.538A>G	ENSP00000419129.1:p.Ile180Val
ENST00000469217.5:c.505A>G	ENSP00000419027.1:p.Ile169Val
ENST00000471595.5:c.445A>G	ENSP00000417549.1:p.Ile149Val
ENST00000473073.1:n.402A>G
ENST00000474833.5:n.168+11409A>G
ENST00000475214.5:n.359A>G
ENST00000478469.5:c.445A>G	ENSP00000420759.1:p.Ile149Val
ENST00000482086.5:c.97A>G	ENSP00000417253.1:p.Ile33Val
ENST00000483687.5:c.388A>G	ENSP00000420639.1:p.Ile130Val
ENST00000484181.5:c.445A>G	ENSP00000417937.1:p.Ile149Val
ENST00000490504.5:c.372+5344A>G	ENSP00000418307.1:n.372+5344A>G
ENST00000494742.5:c.196A>G	ENSP00000418020.1:p.Ile66Val
NM_000532.4:c.445A>G	NP_000523.2:p.Ile149Val
NM_001178014.1:c.505A>G	NP_001171485.1:p.Ile169Val
XM_011512873.1:c.445A>G	XP_011511175.1:p.Ile149Val
XM_011512873.2:c.445A>G	XP_011511175.1:p.Ile149Val
NM_000532.5:c.445A>G MANE Select	NP_000523.2:p.Ile149Val
NM_001178014.2:c.505A>G	NP_001171485.1:p.Ile169Val