Canonical Allele Identifier: CA1557861702
Gene: JMY HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.79262170G= , CM000667.2:g.79262170G= GRCh38
NC_000005.9:g.78557993G= , CM000667.1:g.78557993G= GRCh37
NC_000005.8:g.78593749G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000396137.5:c.1033-15740G= MANE Select ENSP00000379441.4:n.1033-15740G=
ENST00000396137.4:c.1033-15740G= ENSP00000379441.4:n.1033-15740G=
NM_152405.4:c.1033-15740G= NP_689618.4:n.1033-15740G=
XM_005248430.1:c.1033-15740G= XP_005248487.1:n.1033-15740G=
XM_011543155.1:c.1033-15740G= XP_011541457.1:n.1033-15740G=
XM_005248430.3:c.1033-15740G= XP_005248487.1:n.1033-15740G=
XM_011543155.3:c.1033-15740G= XP_011541457.1:n.1033-15740G=
NM_152405.5:c.1033-15740G= MANE Select NP_689618.4:n.1033-15740G=
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