Canonical Allele Identifier: CA814306226

Gene: JMY

Linked Data

• dbSNP Id: rs1442972443
• gnomAD v3: 5-79261987-A-G
• gnomAD v4: 5-79261987-A-G
• MyVariant Identifiers: chr5:g.78557810A>G (hg19) ; chr5:g.79261987A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.79261987A>G , CM000667.2:g.79261987A>G	GRCh38
NC_000005.9:g.78557810A>G , CM000667.1:g.78557810A>G	GRCh37
NC_000005.8:g.78593566A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396137.5:c.1033-15923A>G MANE Select	ENSP00000379441.4:n.1033-15923A>G
ENST00000396137.4:c.1033-15923A>G	ENSP00000379441.4:n.1033-15923A>G
NM_152405.4:c.1033-15923A>G	NP_689618.4:n.1033-15923A>G
XM_005248430.1:c.1033-15923A>G	XP_005248487.1:n.1033-15923A>G
XM_011543155.1:c.1033-15923A>G	XP_011541457.1:n.1033-15923A>G
XM_005248430.3:c.1033-15923A>G	XP_005248487.1:n.1033-15923A>G
XM_011543155.3:c.1033-15923A>G	XP_011541457.1:n.1033-15923A>G
NM_152405.5:c.1033-15923A>G MANE Select	NP_689618.4:n.1033-15923A>G