Canonical Allele Identifier: CA2247220181
Gene: MYH8 HGNC NCBI
MYHAS HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.10404274T= , CM000679.2:g.10404274T= GRCh38
NC_000017.10:g.10307591T= , CM000679.1:g.10307591T= GRCh37
NC_000017.9:g.10248316T= NCBI36
NG_013015.1:g.22677A=

Transcript Alleles

HGVS Amino-acid change
ENST00000403437.2:c.2688+56A= (MYH8) MANE Select ENSP00000384330.2:n.2688+56A=
NM_002472.2:c.2688+56A= (MYH8) NP_002463.2:n.2688+56A=
NR_125367.1:n.77-1874T= (MYHAS)
XM_011523873.1:c.2784+56A= (MYH8) XP_011522175.1:n.2784+56A=
XM_011523874.1:c.2784+56A= (MYH8) XP_011522176.1:n.2784+56A=
NM_002472.3:c.2688+56A= (MYH8) MANE Select NP_002463.2:n.2688+56A=
Search 100 bp 5'
Search 100 bp 3'