Canonical Allele Identifier: CA2247307009

Gene: MYH2 MYHAS

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.10539763C= , CM000679.2:g.10539763C=	GRCh38
NC_000017.10:g.10443080C= , CM000679.1:g.10443080C=	GRCh37
NC_000017.9:g.10383805C=	NCBI36
NG_013014.1:g.14938G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000245503.10:c.1147+165G= (MYH2) MANE Select	ENSP00000245503.5:n.1147+165G=
ENST00000245503.9:c.1147+165G= (MYH2)	ENSP00000245503.5:n.1147+165G=
ENST00000397183.6:c.1147+165G= (MYH2)	ENSP00000380367.2:n.1147+165G=
ENST00000532183.6:c.1147+165G= (MYH2)	ENSP00000433944.1:n.1147+165G=
ENST00000622564.4:c.1147+165G= (MYH2)	ENSP00000482463.1:n.1147+165G=
NM_001100112.1:c.1147+165G= (MYH2)	NP_001093582.1:n.1147+165G=
NM_017534.5:c.1147+165G= (MYH2)	NP_060004.3:n.1147+165G=
NR_125367.1:n.168-27774C= (MYHAS)
NM_017534.6:c.1147+165G= (MYH2) MANE Select	NP_060004.3:n.1147+165G=
NM_001100112.2:c.1147+165G= (MYH2)	NP_001093582.1:n.1147+165G=