Canonical Allele Identifier: CA2636107313
Gene: MYH8 HGNC NCBI
MYHAS HGNC NCBI

Linked Data

gnomAD v4: 17-10404246-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.10404246T>C , CM000679.2:g.10404246T>C GRCh38
NC_000017.10:g.10307563T>C , CM000679.1:g.10307563T>C GRCh37
NC_000017.9:g.10248288T>C NCBI36
NG_013015.1:g.22705A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000403437.2:c.2688+84A>G (MYH8) MANE Select ENSP00000384330.2:n.2688+84A>G
NM_002472.2:c.2688+84A>G (MYH8) NP_002463.2:n.2688+84A>G
NR_125367.1:n.77-1902T>C (MYHAS)
XM_011523873.1:c.2784+84A>G (MYH8) XP_011522175.1:n.2784+84A>G
XM_011523874.1:c.2784+84A>G (MYH8) XP_011522176.1:n.2784+84A>G
NM_002472.3:c.2688+84A>G (MYH8) MANE Select NP_002463.2:n.2688+84A>G
Search 100 bp 5'
Search 100 bp 3'