Canonical Allele Identifier: CA2123468788

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23417367G= , CM000676.2:g.23417367G= GRCh38
NC_000014.8:g.23886576G= , CM000676.1:g.23886576G= GRCh37
NC_000014.7:g.22956416G= NCBI36
NG_007884.1:g.23295C= , LRG_384:g.23295C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4354-49C= (MYH7) MANE Select ENSP00000347507.3:n.4354-49C=
ENST00000355349.3:c.4354-49C= (MYH7) ENSP00000347507.3:n.4354-49C=
NM_000257.3:c.4354-49C= (MYH7) NP_000248.2:n.4354-49C=
NR_126491.1:n.807G= (MHRT)
XM_017021340.1:c.4354-49C= (MYH7) XP_016876829.1:n.4354-49C=
NM_000257.4:c.4354-49C= (MYH7) MANE Select NP_000248.2:n.4354-49C=