Canonical Allele Identifier: CA449801081

Gene: MPIG6B

Linked Data

• dbSNP Id: rs1431175093
• gnomAD v2: 6-31691720-G-A
• MyVariant Identifiers: chr6:g.31691720G>A (hg19) ; chr6:g.31723943G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31723943G>A , CM000668.2:g.31723943G>A	GRCh38
NC_000006.11:g.31691720G>A , CM000668.1:g.31691720G>A	GRCh37
NC_000006.10:g.31799699G>A	NCBI36
NG_029044.1:g.5600G>A
NG_029044.2:g.5600G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649779.1:c.366G>A MANE Select	ENSP00000497720.1:p.Val122=
ENST00000375804.6:c.366G>A	ENSP00000364962.2:p.Val122=
ENST00000375805.6:c.366G>A	ENSP00000364963.2:p.Val122=
ENST00000375806.2:c.366G>A	ENSP00000364964.2:p.Val122=
ENST00000375809.7:c.366G>A	ENSP00000364967.3:p.Val122=
ENST00000375810.8:c.366G>A	ENSP00000364968.4:p.Val122=
ENST00000375814.7:c.366G>A	ENSP00000364972.3:p.Val122=
ENST00000460663.5:n.573G>A
ENST00000466312.5:n.370G>A
ENST00000471545.1:n.366G>A
ENST00000480039.5:c.366G>A	ENSP00000419306.1:p.Val122=
ENST00000485548.5:c.268+98G>A	ENSP00000420355.1:n.268+98G>A
NM_025260.3:c.366G>A	NP_079536.2:p.Val122=
NM_138272.2:c.366G>A	NP_612116.1:p.Val122=
NM_138273.2:c.366G>A	NP_612117.1:p.Val122=
NM_138274.2:c.366G>A	NP_612118.1:p.Val122=
NM_138275.2:c.366G>A	NP_612119.1:p.Val122=
NM_138277.2:c.366G>A	NP_612121.1:p.Val122=
XM_011514920.1:c.414G>A	XP_011513222.1:p.Val138=
XM_011514921.1:c.414G>A	XP_011513223.1:p.Val138=
XM_011514920.2:c.414G>A	XP_011513222.1:p.Val138=
XM_011514921.2:c.414G>A	XP_011513223.1:p.Val138=
XM_017011330.1:c.414G>A	XP_016866819.1:p.Val138=
XM_017011331.1:c.366G>A	XP_016866820.1:p.Val122=
XM_017011332.1:c.414G>A	XP_016866821.1:p.Val138=
XM_017011333.1:c.414G>A	XP_016866822.1:p.Val138=
NM_025260.4:c.366G>A	NP_079536.2:p.Val122=
NM_138272.3:c.366G>A MANE Select	NP_612116.1:p.Val122=
NM_138273.3:c.366G>A	NP_612117.1:p.Val122=
NM_138274.3:c.366G>A	NP_612118.1:p.Val122=
NM_138275.3:c.366G>A	NP_612119.1:p.Val122=
NM_138277.3:c.366G>A	NP_612121.1:p.Val122=