Canonical Allele Identifier: CA1557861693

Gene: JMY

Linked Data

• dbSNP Id: rs1269105407

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.79262150C>G , CM000667.2:g.79262150C>G	GRCh38
NC_000005.9:g.78557973C>G , CM000667.1:g.78557973C>G	GRCh37
NC_000005.8:g.78593729C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396137.5:c.1033-15760C>G MANE Select	ENSP00000379441.4:n.1033-15760C>G
ENST00000396137.4:c.1033-15760C>G	ENSP00000379441.4:n.1033-15760C>G
NM_152405.4:c.1033-15760C>G	NP_689618.4:n.1033-15760C>G
XM_005248430.1:c.1033-15760C>G	XP_005248487.1:n.1033-15760C>G
XM_011543155.1:c.1033-15760C>G	XP_011541457.1:n.1033-15760C>G
XM_005248430.3:c.1033-15760C>G	XP_005248487.1:n.1033-15760C>G
XM_011543155.3:c.1033-15760C>G	XP_011541457.1:n.1033-15760C>G
NM_152405.5:c.1033-15760C>G MANE Select	NP_689618.4:n.1033-15760C>G