Canonical Allele Identifier: CA624877707

Gene: MYH8 MYHAS

Linked Data

• dbSNP Id: rs1432235673
• gnomAD v2: 17-10312406-TACTTTACCCTGA-T
• gnomAD v4: 17-10409089-TACTTTACCCTGA-T
• MyVariant Identifiers: chr17:g.10312407_10312418del (hg19) ; chr17:g.10409090_10409101del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.10409091_10409102del , CM000679.2:g.10409091_10409102del	GRCh38
NC_000017.10:g.10312408_10312419del , CM000679.1:g.10312408_10312419del	GRCh37
NC_000017.9:g.10253133_10253144del	NCBI36
NG_013015.1:g.17850_17861del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403437.2:c.1961_1965+7del (MYH8)
NM_002472.2:c.1961_1965+7del (MYH8)
NR_125367.1:n.167+2853_167+2864del (MYHAS)
XM_011523873.1:c.1961_1965+7del (MYH8)
XM_011523874.1:c.1961_1965+7del (MYH8)
NM_002472.3:c.1961_1965+7del (MYH8)