Canonical Allele Identifier: CA656016741
Gene: MYH7 HGNC NCBI

Linked Data

COSMIC: COSN26578221
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23423488G>T , CM000676.2:g.23423488G>T GRCh38
NC_000014.8:g.23892697G>T , CM000676.1:g.23892697G>T GRCh37
NC_000014.7:g.22962537G>T NCBI36
NG_007884.1:g.17174C>A , LRG_384:g.17174C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3099+59C>A MANE Select ENSP00000347507.3:n.3099+59C>A
ENST00000355349.3:c.3099+59C>A ENSP00000347507.3:n.3099+59C>A
NM_000257.3:c.3099+59C>A NP_000248.2:n.3099+59C>A
XR_245686.3:n.3205+59C>A
XM_017021340.1:c.3099+59C>A XP_016876829.1:n.3099+59C>A
NM_000257.4:c.3099+59C>A MANE Select NP_000248.2:n.3099+59C>A
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