Canonical Allele Identifier: CA449801044
Gene: MPIG6B HGNC NCBI

Linked Data

gnomAD v4: 6-31723907-C-T
MyVariant Identifiers: chr6:g.31691684C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31723907C>T , CM000668.2:g.31723907C>T GRCh38
NC_000006.11:g.31691684C>T , CM000668.1:g.31691684C>T GRCh37
NC_000006.10:g.31799663C>T NCBI36
NG_029044.1:g.5564C>T
NG_029044.2:g.5564C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000649779.1:c.330C>T MANE Select ENSP00000497720.1:p.Gly110=
ENST00000375804.6:c.330C>T ENSP00000364962.2:p.Gly110=
ENST00000375805.6:c.330C>T ENSP00000364963.2:p.Gly110=
ENST00000375806.2:c.330C>T ENSP00000364964.2:p.Gly110=
ENST00000375809.7:c.330C>T ENSP00000364967.3:p.Gly110=
ENST00000375810.8:c.330C>T ENSP00000364968.4:p.Gly110=
ENST00000375814.7:c.330C>T ENSP00000364972.3:p.Gly110=
ENST00000460663.5:n.537C>T
ENST00000466312.5:n.334C>T
ENST00000471545.1:n.330C>T
ENST00000480039.5:c.330C>T ENSP00000419306.1:p.Gly110=
ENST00000485548.5:c.268+62C>T ENSP00000420355.1:n.268+62C>T
NM_025260.3:c.330C>T NP_079536.2:p.Gly110=
NM_138272.2:c.330C>T NP_612116.1:p.Gly110=
NM_138273.2:c.330C>T NP_612117.1:p.Gly110=
NM_138274.2:c.330C>T NP_612118.1:p.Gly110=
NM_138275.2:c.330C>T NP_612119.1:p.Gly110=
NM_138277.2:c.330C>T NP_612121.1:p.Gly110=
XM_011514920.1:c.378C>T XP_011513222.1:p.Gly126=
XM_011514921.1:c.378C>T XP_011513223.1:p.Gly126=
XM_011514920.2:c.378C>T XP_011513222.1:p.Gly126=
XM_011514921.2:c.378C>T XP_011513223.1:p.Gly126=
XM_017011330.1:c.378C>T XP_016866819.1:p.Gly126=
XM_017011331.1:c.330C>T XP_016866820.1:p.Gly110=
XM_017011332.1:c.378C>T XP_016866821.1:p.Gly126=
XM_017011333.1:c.378C>T XP_016866822.1:p.Gly126=
NM_025260.4:c.330C>T NP_079536.2:p.Gly110=
NM_138272.3:c.330C>T MANE Select NP_612116.1:p.Gly110=
NM_138273.3:c.330C>T NP_612117.1:p.Gly110=
NM_138274.3:c.330C>T NP_612118.1:p.Gly110=
NM_138275.3:c.330C>T NP_612119.1:p.Gly110=
NM_138277.3:c.330C>T NP_612121.1:p.Gly110=