Canonical Allele Identifier: CA510293141
Gene: MYH7B HGNC NCBI
MIR499A HGNC NCBI
MIR499B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.34990448A>C , CM000682.2:g.34990448A>C GRCh38
NC_000020.10:g.33578251A>C , CM000682.1:g.33578251A>C GRCh37
NC_000020.9:g.33041912A>C NCBI36
NG_016984.2:g.39548A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262873.13:c.1977+138A>C (MYH7B) MANE Select ENSP00000262873.8:n.1977+138A>C
ENST00000262873.12:c.1977+138A>C (MYH7B) ENSP00000262873.8:n.1977+138A>C
ENST00000618182.6:c.2100+138A>C (MYH7B) ENSP00000483640.3:n.2100+138A>C
ENST00000262873.11:c.2103+138A>C (MYH7B) ENSP00000262873.7:n.2103+138A>C
ENST00000618182.4:c.2100+138A>C (MYH7B) ENSP00000483640.1:n.2100+138A>C
NM_020884.4:c.2103+138A>C (MYH7B) NP_065935.3:n.2103+138A>C
NR_030223.1:n.73A>C (MIR499A)
NR_039912.1:n.25T>G (MIR499B)
XM_006723840.2:c.2103+138A>C (MYH7B) XP_006723903.1:n.2103+138A>C
XM_011528941.1:c.2127+138A>C (MYH7B) XP_011527243.1:n.2127+138A>C
XM_011528942.1:c.2127+138A>C (MYH7B) XP_011527244.1:n.2127+138A>C
XM_011528943.1:c.2067+138A>C (MYH7B) XP_011527245.1:n.2067+138A>C
XM_011528944.1:c.2028+138A>C (MYH7B) XP_011527246.1:n.2028+138A>C
XM_011528945.1:c.1557+138A>C (MYH7B) XP_011527247.1:n.1557+138A>C
XM_011528946.1:c.1545+138A>C (MYH7B) XP_011527248.1:n.1545+138A>C
XM_011528947.1:c.1350+138A>C (MYH7B) XP_011527249.1:n.1350+138A>C
XM_011528948.1:c.1350+138A>C (MYH7B) XP_011527250.1:n.1350+138A>C
XM_011528950.1:c.2127+138A>C (MYH7B) XP_011527252.1:n.2127+138A>C
XM_006723840.3:c.2103+138A>C (MYH7B) XP_006723903.1:n.2103+138A>C
XM_011528941.2:c.2127+138A>C (MYH7B) XP_011527243.1:n.2127+138A>C
XM_011528947.2:c.1350+138A>C (MYH7B) XP_011527249.1:n.1350+138A>C
XM_011528948.2:c.1350+138A>C (MYH7B) XP_011527250.1:n.1350+138A>C
XM_017027986.1:c.2163+138A>C (MYH7B) XP_016883475.1:n.2163+138A>C
XR_001754582.1:n.94+472T>G
NM_020884.5:c.2103+138A>C (MYH7B) NP_065935.3:n.2103+138A>C
NM_020884.7:c.1977+138A>C (MYH7B) MANE Select NP_065935.4:n.1977+138A>C
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