Canonical Allele Identifier: CA1557861635
Gene: JMY HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.79261999T= , CM000667.2:g.79261999T= GRCh38
NC_000005.9:g.78557822T= , CM000667.1:g.78557822T= GRCh37
NC_000005.8:g.78593578T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000396137.5:c.1033-15911T= MANE Select ENSP00000379441.4:n.1033-15911T=
ENST00000396137.4:c.1033-15911T= ENSP00000379441.4:n.1033-15911T=
NM_152405.4:c.1033-15911T= NP_689618.4:n.1033-15911T=
XM_005248430.1:c.1033-15911T= XP_005248487.1:n.1033-15911T=
XM_011543155.1:c.1033-15911T= XP_011541457.1:n.1033-15911T=
XM_005248430.3:c.1033-15911T= XP_005248487.1:n.1033-15911T=
XM_011543155.3:c.1033-15911T= XP_011541457.1:n.1033-15911T=
NM_152405.5:c.1033-15911T= MANE Select NP_689618.4:n.1033-15911T=
Search 100 bp 5'
Search 100 bp 3'