Canonical Allele Identifier: CA2756108489
Gene: MYL3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46858275_46858385del , CM000665.2:g.46858275_46858385del GRCh38
NC_000003.11:g.46899765_46899875del , CM000665.1:g.46899765_46899875del GRCh37
NC_000003.10:g.46874769_46874879del NCBI36
NG_007555.2:g.28787_28897del , LRG_395:g.28787_28897del

Transcript Alleles

HGVS Amino-acid Change
ENST00000431168.2:c.559+1_560-1del
ENST00000292327.6:c.559+1_560-1del
ENST00000653454.1:c.559+1_560-1del
ENST00000654597.1:c.559+1_560-1del
ENST00000655244.1:n.766+1_767-1del
ENST00000662933.1:c.559+1_560-1del
ENST00000664891.1:n.517+1_518-1del
ENST00000292327.4:c.559+1_560-1del
ENST00000395869.5:c.559+1_560-1del
NM_000258.2:c.559+1_560-1del , LRG_395t1:c.559+1_560-1del
NM_000258.3:c.559+1_560-1del
Search 100 bp 5'
Search 100 bp 3'