Canonical Allele Identifier: CA402428669
Gene: MYO5B HGNC NCBI

Linked Data

dbSNP Id: rs2024556287
MyVariant Identifiers: chr18:g.47405319A>G (hg19) chr18:g.49878949A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.49878949A>G , CM000680.2:g.49878949A>G GRCh38
NC_000018.9:g.47405319A>G , CM000680.1:g.47405319A>G GRCh37
NC_000018.8:g.45659317A>G NCBI36
NG_012925.1:g.321133T>C
NG_012925.2:g.321133T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000697218.1:n.26T>C
ENST00000697219.1:c.3069T>C
ENST00000285039.12:c.3272T>C MANE Select ENSP00000285039.6:p.Ile1091Thr
ENST00000285039.11:c.3272T>C ENSP00000285039.6:p.Ile1091Thr
ENST00000324581.10:c.701T>C ENSP00000315531.7:p.Ile234Thr
ENST00000589568.1:n.473T>C
ENST00000616031.4:c.1907-42216T>C ENSP00000479038.1:n.1907-42216T>C
NM_001080467.2:c.3272T>C NP_001073936.1:p.Ile1091Thr
NM_001080467.3:c.3272T>C MANE Select NP_001073936.1:p.Ile1091Thr
Search 100 bp 5'
Search 100 bp 3'