Canonical Allele Identifier: CA624877701

Gene: MYH8 MYHAS

Linked Data

• dbSNP Id: rs1406479143
• gnomAD v2: 17-10312381-G-C
• gnomAD v3: 17-10409064-G-C
• gnomAD v4: 17-10409064-G-C
• MyVariant Identifiers: chr17:g.10312381G>C (hg19) ; chr17:g.10409064G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.10409064G>C , CM000679.2:g.10409064G>C	GRCh38
NC_000017.10:g.10312381G>C , CM000679.1:g.10312381G>C	GRCh37
NC_000017.9:g.10253106G>C	NCBI36
NG_013015.1:g.17887C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403437.2:c.1965+33C>G (MYH8) MANE Select	ENSP00000384330.2:n.1965+33C>G
NM_002472.2:c.1965+33C>G (MYH8)	NP_002463.2:n.1965+33C>G
NR_125367.1:n.167+2826G>C (MYHAS)
XM_011523873.1:c.1965+33C>G (MYH8)	XP_011522175.1:n.1965+33C>G
XM_011523874.1:c.1965+33C>G (MYH8)	XP_011522176.1:n.1965+33C>G
NM_002472.3:c.1965+33C>G (MYH8) MANE Select	NP_002463.2:n.1965+33C>G