Canonical Allele Identifier: CA2652580966

Gene: MYH7B

Linked Data

• gnomAD v4: 20-34977958-AACCT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.34977959_34977962del , CM000682.2:g.34977959_34977962del	GRCh38
NC_000020.10:g.33565762_33565765del , CM000682.1:g.33565762_33565765del	GRCh37
NC_000020.9:g.33029423_33029426del	NCBI36
NG_016984.2:g.27059_27062del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262873.13:c.-47_-44del MANE Select	ENSP00000262873.8:n.-47_-44del
ENST00000262873.12:c.-47_-44del	ENSP00000262873.8:n.-47_-44del
ENST00000618182.6:c.77_80del	ENSP00000483640.3:p.Asn26ThrfsTer16
ENST00000673749.1:n.488_491del
ENST00000262873.11:c.80_83del	ENSP00000262873.7:p.Asn27ThrfsTer16
ENST00000470929.5:n.40_43del
ENST00000618182.4:c.77_80del	ENSP00000483640.1:p.Asn26ThrfsTer16
NM_020884.4:c.80_83del	NP_065935.3:p.Asn27ThrfsTer16
XM_006723840.2:c.80_83del	XP_006723903.1:p.Asn27ThrfsTer16
XM_011528941.1:c.80_83del	XP_011527243.1:p.Asn27ThrfsTer16
XM_011528942.1:c.80_83del	XP_011527244.1:p.Asn27ThrfsTer16
XM_011528943.1:c.80_83del	XP_011527245.1:p.Asn27ThrfsTer16
XM_011528944.1:c.80_83del	XP_011527246.1:p.Asn27ThrfsTer16
XM_011528945.1:c.-430_-427del	XP_011527247.1:n.-430_-427del
XM_011528950.1:c.80_83del	XP_011527252.1:p.Asn27ThrfsTer16
XM_006723840.3:c.80_83del	XP_006723903.1:p.Asn27ThrfsTer16
XM_011528941.2:c.80_83del	XP_011527243.1:p.Asn27ThrfsTer16
XM_017027986.1:c.80_83del	XP_016883475.1:p.Asn27ThrfsTer16
NM_020884.5:c.80_83del	NP_065935.3:p.Asn27ThrfsTer16
NM_020884.7:c.-47_-44del MANE Select	NP_065935.4:n.-47_-44del