Canonical Allele Identifier: CA398148019

Gene: MYH2 MYHAS

Linked Data

• MyVariant Identifiers: chr17:g.10436638A>C (hg19) ; chr17:g.10533321A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.10533321A>C , CM000679.2:g.10533321A>C	GRCh38
NC_000017.10:g.10436638A>C , CM000679.1:g.10436638A>C	GRCh37
NC_000017.9:g.10377363A>C	NCBI36
NG_013014.1:g.21380T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000245503.10:c.2405T>G (MYH2) MANE Select	ENSP00000245503.5:p.Leu802Trp
ENST00000245503.9:c.2405T>G (MYH2)	ENSP00000245503.5:p.Leu802Trp
ENST00000397183.6:c.2405T>G (MYH2)	ENSP00000380367.2:p.Leu802Trp
ENST00000532183.6:c.1974+3209T>G (MYH2)	ENSP00000433944.1:n.1974+3209T>G
ENST00000622564.4:c.1974+3209T>G (MYH2)	ENSP00000482463.1:n.1974+3209T>G
NM_001100112.1:c.2405T>G (MYH2)	NP_001093582.1:p.Leu802Trp
NM_017534.5:c.2405T>G (MYH2)	NP_060004.3:p.Leu802Trp
NR_125367.1:n.168-34216A>C (MYHAS)
NM_017534.6:c.2405T>G (MYH2) MANE Select	NP_060004.3:p.Leu802Trp
NM_001100112.2:c.2405T>G (MYH2)	NP_001093582.1:p.Leu802Trp