Canonical Allele Identifier: CA2302428756
Gene: MYO5B HGNC NCBI

Linked Data

dbSNP Id: rs2024556060

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.49878940dup , CM000680.2:g.49878940dup GRCh38
NC_000018.9:g.47405310dup , CM000680.1:g.47405310dup GRCh37
NC_000018.8:g.45659308dup NCBI36
NG_012925.1:g.321147dup
NG_012925.2:g.321147dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000697218.1:n.40dup
ENST00000697219.1:c.3073+10dup
ENST00000285039.12:c.3276+10dup MANE Select ENSP00000285039.6:n.3276+10dup
ENST00000285039.11:c.3276+10dup ENSP00000285039.6:n.3276+10dup
ENST00000324581.10:c.705+10dup ENSP00000315531.7:n.705+10dup
ENST00000589568.1:n.477+10dup
ENST00000616031.4:c.1907-42202dup ENSP00000479038.1:n.1907-42202dup
NM_001080467.2:c.3276+10dup NP_001073936.1:n.3276+10dup
NM_001080467.3:c.3276+10dup MANE Select NP_001073936.1:n.3276+10dup