Canonical Allele Identifier: CA2636109479
Gene: MYH3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.10639801_10639805del , CM000679.2:g.10639801_10639805del GRCh38
NC_000017.10:g.10543118_10543122del , CM000679.1:g.10543118_10543122del GRCh37
NC_000017.9:g.10483843_10483847del NCBI36
NG_011537.1:g.22497_22501del

Transcript Alleles

HGVS Amino-acid Change
ENST00000583535.6:c.2683_2687del
ENST00000583535.5:c.2683_2687del
NM_002470.3:c.2683_2687del
XM_011523870.1:c.2683_2687del
XM_011523871.1:c.2683_2687del
XM_011523872.1:c.2683_2687del
XM_011523870.3:c.2683_2687del
XM_011523871.2:c.2683_2687del
NM_002470.4:c.2683_2687del