Canonical Allele Identifier: CA257825492
Gene: MYH7 HGNC NCBI

Linked Data

dbSNP Id: rs112573292
gnomAD v2: 14-23899925-G-T
gnomAD v3: 14-23430716-G-T
gnomAD v4: 14-23430716-G-T
MyVariant Identifiers: chr14:g.23899925G>T (hg19) chr14:g.23430716G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23430716G>T , CM000676.2:g.23430716G>T GRCh38
NC_000014.8:g.23899925G>T , CM000676.1:g.23899925G>T GRCh37
NC_000014.7:g.22969765G>T NCBI36
NG_007884.1:g.9946C>A , LRG_384:g.9946C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.896-53C>A MANE Select ENSP00000347507.3:n.896-53C>A
ENST00000355349.3:c.896-53C>A ENSP00000347507.3:n.896-53C>A
NM_000257.3:c.896-53C>A NP_000248.2:n.896-53C>A
XR_245686.3:n.1002-53C>A
XM_017021340.1:c.896-53C>A XP_016876829.1:n.896-53C>A
NM_000257.4:c.896-53C>A MANE Select NP_000248.2:n.896-53C>A
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