Canonical Allele Identifier: CA510290202

Gene: MYH7B

Linked Data

• MyVariant Identifiers: chr20:g.33565766C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.34977963C>G , CM000682.2:g.34977963C>G	GRCh38
NC_000020.10:g.33565766C>G , CM000682.1:g.33565766C>G	GRCh37
NC_000020.9:g.33029427C>G	NCBI36
NG_016984.2:g.27063C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262873.13:c.-43C>G MANE Select	ENSP00000262873.8:n.-43C>G
ENST00000262873.12:c.-43C>G	ENSP00000262873.8:n.-43C>G
ENST00000618182.6:c.81C>G	ENSP00000483640.3:p.Leu27=
ENST00000673749.1:n.492C>G
ENST00000262873.11:c.84C>G	ENSP00000262873.7:p.Leu28=
ENST00000470929.5:n.44C>G
ENST00000618182.4:c.81C>G	ENSP00000483640.1:p.Leu27=
NM_020884.4:c.84C>G	NP_065935.3:p.Leu28=
XM_006723840.2:c.84C>G	XP_006723903.1:p.Leu28=
XM_011528941.1:c.84C>G	XP_011527243.1:p.Leu28=
XM_011528942.1:c.84C>G	XP_011527244.1:p.Leu28=
XM_011528943.1:c.84C>G	XP_011527245.1:p.Leu28=
XM_011528944.1:c.84C>G	XP_011527246.1:p.Leu28=
XM_011528945.1:c.-426C>G	XP_011527247.1:n.-426C>G
XM_011528950.1:c.84C>G	XP_011527252.1:p.Leu28=
XM_006723840.3:c.84C>G	XP_006723903.1:p.Leu28=
XM_011528941.2:c.84C>G	XP_011527243.1:p.Leu28=
XM_017027986.1:c.84C>G	XP_016883475.1:p.Leu28=
NM_020884.5:c.84C>G	NP_065935.3:p.Leu28=
NM_020884.7:c.-43C>G MANE Select	NP_065935.4:n.-43C>G