Canonical Allele Identifier: CA485617441
Gene: MYH7 HGNC NCBI
MHRT HGNC NCBI

Linked Data

ClinVar Variation Id: 2773898
ClinVar RCV Id: RCV003532661
MyVariant Identifiers: chr14:g.23886447G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23417238G>A , CM000676.2:g.23417238G>A GRCh38
NC_000014.8:g.23886447G>A , CM000676.1:g.23886447G>A GRCh37
NC_000014.7:g.22956287G>A NCBI36
NG_007884.1:g.23424C>T , LRG_384:g.23424C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4434C>T (MYH7) MANE Select ENSP00000347507.3:p.Ser1478=
ENST00000355349.3:c.4434C>T (MYH7) ENSP00000347507.3:p.Ser1478=
NM_000257.3:c.4434C>T (MYH7) NP_000248.2:p.Ser1478=
NR_126491.1:n.678G>A (MHRT)
XM_017021340.1:c.4434C>T (MYH7) XP_016876829.1:p.Ser1478=
NM_000257.4:c.4434C>T (MYH7) MANE Select NP_000248.2:p.Ser1478=
Search 100 bp 5'
Search 100 bp 3'