Canonical Allele Identifier: CA354650101

Gene: PCCB

Linked Data

• MyVariant Identifiers: chr3:g.136048799T>G (hg19) ; chr3:g.136329957T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.136329957T>G , CM000665.2:g.136329957T>G	GRCh38
NC_000003.11:g.136048799T>G , CM000665.1:g.136048799T>G	GRCh37
NC_000003.10:g.137531489T>G	NCBI36
NG_008939.1:g.84633T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000251654.9:c.1551T>G MANE Select	ENSP00000251654.4:p.Cys517Trp
ENST00000251654.8:c.1551T>G	ENSP00000251654.4:p.Cys517Trp
ENST00000462637.5:c.1482T>G	ENSP00000420391.1:p.Cys494Trp
ENST00000466072.5:c.1611T>G	ENSP00000420158.1:p.Cys537Trp
ENST00000468777.5:c.1644T>G	ENSP00000419129.1:p.Cys548Trp
ENST00000469217.5:c.1611T>G	ENSP00000419027.1:p.Cys537Trp
ENST00000471595.5:c.1551T>G	ENSP00000417549.1:p.Cys517Trp
ENST00000473073.1:n.1752T>G
ENST00000478469.5:c.885-4323T>G	ENSP00000420759.1:n.885-4323T>G
ENST00000482086.5:c.1203T>G	ENSP00000417253.1:p.Cys401Trp
ENST00000483687.5:c.1494T>G	ENSP00000420639.1:p.Cys498Trp
ENST00000484181.5:c.*232T>G	ENSP00000417937.1:n.*232T>G
ENST00000490504.5:c.1380T>G	ENSP00000418307.1:p.Cys460Trp
NM_000532.4:c.1551T>G	NP_000523.2:p.Cys517Trp
NM_001178014.1:c.1611T>G	NP_001171485.1:p.Cys537Trp
NM_000532.5:c.1551T>G MANE Select	NP_000523.2:p.Cys517Trp
NM_001178014.2:c.1611T>G	NP_001171485.1:p.Cys537Trp