Canonical Allele Identifier: CA2665478455
Gene: MYL3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46859476del , CM000665.2:g.46859476del GRCh38
NC_000003.11:g.46900966del , CM000665.1:g.46900966del GRCh37
NC_000003.10:g.46875970del NCBI36
NG_007555.2:g.27696del , LRG_395:g.27696del

Transcript Alleles

HGVS Amino-acid change
ENST00000431168.2:c.481+1del
ENST00000292327.6:c.481+1del
ENST00000653454.1:c.481+1del
ENST00000654597.1:c.481+1del
ENST00000655244.1:n.703+1del
ENST00000662933.1:c.481+1del
ENST00000664891.1:n.439+1del
ENST00000292327.4:c.481+1del
ENST00000395869.5:c.481+1del
NM_000258.2:c.481+1del , LRG_395t1:c.481+1del
NM_000258.3:c.481+1del