Canonical Allele Identifier: CA435957029

Gene: PCCB

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.136250393G>C , CM000665.2:g.136250393G>C	GRCh38
NC_000003.11:g.135969235G>C , CM000665.1:g.135969235G>C	GRCh37
NC_000003.10:g.137451925G>C	NCBI36
NG_008939.1:g.5069G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251654.9:c.18G>C MANE Select	ENSP00000251654.4:p.Arg6=
ENST00000251654.8:c.18G>C	ENSP00000251654.4:p.Arg6=
ENST00000462637.5:c.18G>C	ENSP00000420391.1:p.Arg6=
ENST00000465423.5:c.18G>C	ENSP00000419263.1:p.Arg6=
ENST00000466072.5:c.18G>C	ENSP00000420158.1:p.Arg6=
ENST00000468777.5:c.18G>C	ENSP00000419129.1:p.Arg6=
ENST00000469217.5:c.18G>C	ENSP00000419027.1:p.Arg6=
ENST00000471595.5:c.18G>C	ENSP00000417549.1:p.Arg6=
ENST00000474833.5:n.3G>C
ENST00000478469.5:c.18G>C	ENSP00000420759.1:p.Arg6=
ENST00000482086.5:c.18G>C	ENSP00000417253.1:p.Arg6=
ENST00000483687.5:c.18G>C	ENSP00000420639.1:p.Arg6=
ENST00000484181.5:c.18G>C	ENSP00000417937.1:p.Arg6=
ENST00000490504.5:c.18G>C	ENSP00000418307.1:p.Arg6=
NM_000532.4:c.18G>C	NP_000523.2:p.Arg6=
NM_001178014.1:c.18G>C	NP_001171485.1:p.Arg6=
XM_011512873.1:c.18G>C	XP_011511175.1:p.Arg6=
XM_011512873.2:c.18G>C	XP_011511175.1:p.Arg6=
NM_000532.5:c.18G>C MANE Select	NP_000523.2:p.Arg6=
NM_001178014.2:c.18G>C	NP_001171485.1:p.Arg6=