Canonical Allele Identifier: CA1557861696

Gene: JMY

Linked Data

• dbSNP Id: rs1745442974

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.79262154G>A , CM000667.2:g.79262154G>A	GRCh38
NC_000005.9:g.78557977G>A , CM000667.1:g.78557977G>A	GRCh37
NC_000005.8:g.78593733G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396137.5:c.1033-15756G>A MANE Select	ENSP00000379441.4:n.1033-15756G>A
ENST00000396137.4:c.1033-15756G>A	ENSP00000379441.4:n.1033-15756G>A
NM_152405.4:c.1033-15756G>A	NP_689618.4:n.1033-15756G>A
XM_005248430.1:c.1033-15756G>A	XP_005248487.1:n.1033-15756G>A
XM_011543155.1:c.1033-15756G>A	XP_011541457.1:n.1033-15756G>A
XM_005248430.3:c.1033-15756G>A	XP_005248487.1:n.1033-15756G>A
XM_011543155.3:c.1033-15756G>A	XP_011541457.1:n.1033-15756G>A
NM_152405.5:c.1033-15756G>A MANE Select	NP_689618.4:n.1033-15756G>A