Canonical Allele Identifier: CA2247307007

Gene: MYH2 MYHAS

Linked Data

• dbSNP Id: rs2073528712

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.10539762C>A , CM000679.2:g.10539762C>A	GRCh38
NC_000017.10:g.10443079C>A , CM000679.1:g.10443079C>A	GRCh37
NC_000017.9:g.10383804C>A	NCBI36
NG_013014.1:g.14939G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000245503.10:c.1147+166G>T (MYH2) MANE Select	ENSP00000245503.5:n.1147+166G>T
ENST00000245503.9:c.1147+166G>T (MYH2)	ENSP00000245503.5:n.1147+166G>T
ENST00000397183.6:c.1147+166G>T (MYH2)	ENSP00000380367.2:n.1147+166G>T
ENST00000532183.6:c.1147+166G>T (MYH2)	ENSP00000433944.1:n.1147+166G>T
ENST00000622564.4:c.1147+166G>T (MYH2)	ENSP00000482463.1:n.1147+166G>T
NM_001100112.1:c.1147+166G>T (MYH2)	NP_001093582.1:n.1147+166G>T
NM_017534.5:c.1147+166G>T (MYH2)	NP_060004.3:n.1147+166G>T
NR_125367.1:n.168-27775C>A (MYHAS)
NM_017534.6:c.1147+166G>T (MYH2) MANE Select	NP_060004.3:n.1147+166G>T
NM_001100112.2:c.1147+166G>T (MYH2)	NP_001093582.1:n.1147+166G>T