Canonical Allele Identifier: CA449801046

Gene: MPIG6B

Linked Data

• MyVariant Identifiers: chr6:g.31691687C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31723910C>T , CM000668.2:g.31723910C>T	GRCh38
NC_000006.11:g.31691687C>T , CM000668.1:g.31691687C>T	GRCh37
NC_000006.10:g.31799666C>T	NCBI36
NG_029044.1:g.5567C>T
NG_029044.2:g.5567C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000649779.1:c.333C>T MANE Select	ENSP00000497720.1:p.Arg111=
ENST00000375804.6:c.333C>T	ENSP00000364962.2:p.Arg111=
ENST00000375805.6:c.333C>T	ENSP00000364963.2:p.Arg111=
ENST00000375806.2:c.333C>T	ENSP00000364964.2:p.Arg111=
ENST00000375809.7:c.333C>T	ENSP00000364967.3:p.Arg111=
ENST00000375810.8:c.333C>T	ENSP00000364968.4:p.Arg111=
ENST00000375814.7:c.333C>T	ENSP00000364972.3:p.Arg111=
ENST00000460663.5:n.540C>T
ENST00000466312.5:n.337C>T
ENST00000471545.1:n.333C>T
ENST00000480039.5:c.333C>T	ENSP00000419306.1:p.Arg111=
ENST00000485548.5:c.268+65C>T	ENSP00000420355.1:n.268+65C>T
NM_025260.3:c.333C>T	NP_079536.2:p.Arg111=
NM_138272.2:c.333C>T	NP_612116.1:p.Arg111=
NM_138273.2:c.333C>T	NP_612117.1:p.Arg111=
NM_138274.2:c.333C>T	NP_612118.1:p.Arg111=
NM_138275.2:c.333C>T	NP_612119.1:p.Arg111=
NM_138277.2:c.333C>T	NP_612121.1:p.Arg111=
XM_011514920.1:c.381C>T	XP_011513222.1:p.Arg127=
XM_011514921.1:c.381C>T	XP_011513223.1:p.Arg127=
XM_011514920.2:c.381C>T	XP_011513222.1:p.Arg127=
XM_011514921.2:c.381C>T	XP_011513223.1:p.Arg127=
XM_017011330.1:c.381C>T	XP_016866819.1:p.Arg127=
XM_017011331.1:c.333C>T	XP_016866820.1:p.Arg111=
XM_017011332.1:c.381C>T	XP_016866821.1:p.Arg127=
XM_017011333.1:c.381C>T	XP_016866822.1:p.Arg127=
NM_025260.4:c.333C>T	NP_079536.2:p.Arg111=
NM_138272.3:c.333C>T MANE Select	NP_612116.1:p.Arg111=
NM_138273.3:c.333C>T	NP_612117.1:p.Arg111=
NM_138274.3:c.333C>T	NP_612118.1:p.Arg111=
NM_138275.3:c.333C>T	NP_612119.1:p.Arg111=
NM_138277.3:c.333C>T	NP_612121.1:p.Arg111=