Canonical Allele Identifier: CA408707777

Gene: MYH7B

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.34994403T>A , CM000682.2:g.34994403T>A	GRCh38
NC_000020.10:g.33582206T>A , CM000682.1:g.33582206T>A	GRCh37
NC_000020.9:g.33045867T>A	NCBI36
NG_016984.2:g.43503T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_020884.7:c.2700+2T>A MANE Select	NP_065935.4:n.2700+2T>A
ENST00000262873.13:c.2700+2T>A MANE Select	ENSP00000262873.8:n.2700+2T>A
NM_020884.4:c.2826+2T>A	NP_065935.3:n.2826+2T>A
NM_020884.5:c.2826+2T>A	NP_065935.3:n.2826+2T>A
ENST00000262873.11:c.2826+2T>A	ENSP00000262873.7:n.2826+2T>A
ENST00000262873.12:c.2700+2T>A	ENSP00000262873.8:n.2700+2T>A
ENST00000618182.4:c.2823+2T>A	ENSP00000483640.1:n.2823+2T>A
ENST00000618182.6:c.2823+2T>A	ENSP00000483640.3:n.2823+2T>A
XM_006723840.2:c.2826+2T>A	XP_006723903.1:n.2826+2T>A
XM_006723840.3:c.2826+2T>A	XP_006723903.1:n.2826+2T>A
XM_011528941.1:c.2850+2T>A	XP_011527243.1:n.2850+2T>A
XM_011528941.2:c.2850+2T>A	XP_011527243.1:n.2850+2T>A
XM_011528942.1:c.2850+2T>A	XP_011527244.1:n.2850+2T>A
XM_011528943.1:c.2790+2T>A	XP_011527245.1:n.2790+2T>A
XM_011528944.1:c.2751+2T>A	XP_011527246.1:n.2751+2T>A
XM_011528945.1:c.2280+2T>A	XP_011527247.1:n.2280+2T>A
XM_011528946.1:c.2268+2T>A	XP_011527248.1:n.2268+2T>A
XM_011528947.1:c.2073+2T>A	XP_011527249.1:n.2073+2T>A
XM_011528947.2:c.2073+2T>A	XP_011527249.1:n.2073+2T>A
XM_011528948.1:c.2073+2T>A	XP_011527250.1:n.2073+2T>A
XM_011528948.2:c.2073+2T>A	XP_011527250.1:n.2073+2T>A
XM_011528949.1:c.300+2T>A	XP_011527251.1:n.300+2T>A
XM_011528950.1:c.2850+2T>A	XP_011527252.1:n.2850+2T>A
XM_017027986.1:c.2886+2T>A	XP_016883475.1:n.2886+2T>A