Canonical Allele Identifier: CA9827603

Gene: MYH7B

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.34996486C>T , CM000682.2:g.34996486C>T	GRCh38
NC_000020.10:g.33584289C>T , CM000682.1:g.33584289C>T	GRCh37
NC_000020.9:g.33047950C>T	NCBI36
NG_016984.2:g.45586C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_020884.7:c.3084C>T MANE Select	NP_065935.4:p.Thr1028=
ENST00000262873.13:c.3084C>T MANE Select	ENSP00000262873.8:p.Thr1028=
NM_020884.4:c.3210C>T	NP_065935.3:p.Thr1070=
NM_020884.5:c.3210C>T	NP_065935.3:p.Thr1070=
ENST00000262873.11:c.3210C>T	ENSP00000262873.7:p.Thr1070=
ENST00000262873.12:c.3084C>T	ENSP00000262873.8:p.Thr1028=
ENST00000618182.4:c.3207C>T	ENSP00000483640.1:p.Thr1069=
ENST00000618182.6:c.3207C>T	ENSP00000483640.3:p.Thr1069=
XM_006723840.2:c.3210C>T	XP_006723903.1:p.Thr1070=
XM_006723840.3:c.3210C>T	XP_006723903.1:p.Thr1070=
XM_011528941.1:c.3234C>T	XP_011527243.1:p.Thr1078=
XM_011528941.2:c.3234C>T	XP_011527243.1:p.Thr1078=
XM_011528942.1:c.3234C>T	XP_011527244.1:p.Thr1078=
XM_011528943.1:c.3174C>T	XP_011527245.1:p.Thr1058=
XM_011528944.1:c.3135C>T	XP_011527246.1:p.Thr1045=
XM_011528945.1:c.2664C>T	XP_011527247.1:p.Thr888=
XM_011528946.1:c.2652C>T	XP_011527248.1:p.Thr884=
XM_011528947.1:c.2457C>T	XP_011527249.1:p.Thr819=
XM_011528947.2:c.2457C>T	XP_011527249.1:p.Thr819=
XM_011528948.1:c.2457C>T	XP_011527250.1:p.Thr819=
XM_011528948.2:c.2457C>T	XP_011527250.1:p.Thr819=
XM_011528949.1:c.684C>T	XP_011527251.1:p.Thr228=
XM_017027986.1:c.3270C>T	XP_016883475.1:p.Thr1090=