Canonical Allele Identifier: CA3897747

Gene: MYO6

Linked Data

• dbSNP Id: rs763284731
• ExAC: 6:76623846 G / A
• gnomAD v2: 6-76623846-G-A
• gnomAD v3: 6-75914129-G-A
• gnomAD v4: 6-75914129-G-A
• COSMIC: COSM3875615 ; COSM3875616
• MyVariant Identifiers: chr6:g.76623846G>A (hg19) ; chr6:g.75914129G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.75914129G>A , CM000668.2:g.75914129G>A	GRCh38
NC_000006.11:g.76623846G>A , CM000668.1:g.76623846G>A	GRCh37
NC_000006.10:g.76680566G>A	NCBI36
NG_009934.1:g.169938G>A
NG_009934.2:g.169937G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000369975.6:c.3410G>A	ENSP00000358992.1:p.Arg1137His
ENST00000369977.8:c.3506G>A MANE Select	ENSP00000358994.3:p.Arg1169His
ENST00000369985.9:c.3437G>A	ENSP00000359002.3:p.Arg1146His
ENST00000664640.1:c.3533G>A	ENSP00000499278.1:p.Arg1178His
ENST00000671923.1:c.*1517G>A	ENSP00000500835.1:n.*1517G>A
ENST00000672093.1:c.3506G>A	ENSP00000500710.1:p.Arg1169His
ENST00000672162.1:n.1672G>A
ENST00000369975.5:c.3410G>A	ENSP00000358992.1:p.Arg1137His
ENST00000369977.7:c.3506G>A	ENSP00000358994.3:p.Arg1169His
ENST00000369981.7:c.3536G>A	ENSP00000358998.4:p.Arg1179His
ENST00000369985.8:c.3437G>A	ENSP00000359002.3:p.Arg1146His
ENST00000615563.4:c.3437G>A	ENSP00000478013.1:p.Arg1146His
ENST00000627432.2:c.3533G>A	ENSP00000487348.1:p.Arg1178His
NM_001300899.1:c.3437G>A	NP_001287828.1:p.Arg1146His
NM_004999.3:c.3506G>A	NP_004990.3:p.Arg1169His
XM_005248719.2:c.3533G>A	XP_005248776.1:p.Arg1178His
XM_005248720.2:c.3506G>A	XP_005248777.1:p.Arg1169His
XM_005248721.2:c.3494G>A	XP_005248778.1:p.Arg1165His
XM_005248722.2:c.3479G>A	XP_005248779.1:p.Arg1160His
XM_005248724.2:c.3467G>A	XP_005248781.1:p.Arg1156His
XM_005248726.2:c.3410G>A	XP_005248783.1:p.Arg1137His
XM_005248719.4:c.3533G>A	XP_005248776.1:p.Arg1178His
XM_005248720.4:c.3506G>A	XP_005248777.1:p.Arg1169His
XM_005248721.4:c.3494G>A	XP_005248778.1:p.Arg1165His
XM_005248722.4:c.3479G>A	XP_005248779.1:p.Arg1160His
XM_005248724.4:c.3467G>A	XP_005248781.1:p.Arg1156His
XM_005248726.4:c.3410G>A	XP_005248783.1:p.Arg1137His
XM_017010899.2:c.3440G>A	XP_016866388.1:p.Arg1147His
XM_024446447.1:c.3533G>A	XP_024302215.1:p.Arg1178His
XM_024446448.1:c.3467G>A	XP_024302216.1:p.Arg1156His
NM_004999.4:c.3506G>A MANE Select	NP_004990.3:p.Arg1169His
NM_001300899.2:c.3437G>A	NP_001287828.1:p.Arg1146His
NM_001368136.1:c.3410G>A	NP_001355065.1:p.Arg1137His
NM_001368137.1:c.3467G>A	NP_001355066.1:p.Arg1156His
NM_001368138.1:c.3422G>A	NP_001355067.1:p.Arg1141His
NM_001368865.1:c.3533G>A	NP_001355794.1:p.Arg1178His
NM_001368866.1:c.3506G>A	NP_001355795.1:p.Arg1169His
NR_160538.1:n.3735G>A