Canonical Allele Identifier: CA2123441765
Gene: MYH7 HGNC NCBI

Linked Data

dbSNP Id: rs1892287870
gnomAD v4: 14-23417797-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23417797C>A , CM000676.2:g.23417797C>A GRCh38
NC_000014.8:g.23887006C>A , CM000676.1:g.23887006C>A GRCh37
NC_000014.7:g.22956846C>A NCBI36
NG_007884.1:g.22865G>T , LRG_384:g.22865G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4170-111G>T MANE Select ENSP00000347507.3:n.4170-111G>T
ENST00000355349.3:c.4170-111G>T ENSP00000347507.3:n.4170-111G>T
NM_000257.3:c.4170-111G>T NP_000248.2:n.4170-111G>T
XM_017021340.1:c.4170-111G>T XP_016876829.1:n.4170-111G>T
NM_000257.4:c.4170-111G>T MANE Select NP_000248.2:n.4170-111G>T
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