Canonical Allele Identifier: CA782606006

Gene: ZNF516

Linked Data

• dbSNP Id: rs1179885192
• gnomAD v3: 18-76389998-A-G
• gnomAD v4: 18-76389998-A-G
• MyVariant Identifiers: chr18:g.74101954A>G (hg19) ; chr18:g.76389998A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.76389998A>G , CM000680.2:g.76389998A>G	GRCh38
NC_000018.9:g.74101954A>G , CM000680.1:g.74101954A>G	GRCh37
NC_000018.8:g.72230942A>G	NCBI36
NG_032949.1:g.110193T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000443185.7:c.1811-9695T>C MANE Select	ENSP00000394757.2:n.1811-9695T>C
ENST00000443185.6:c.1811-9695T>C	ENSP00000394757.2:n.1811-9695T>C
NM_014643.3:c.1811-9695T>C	NP_055458.1:n.1811-9695T>C
XM_011526269.1:c.1811-9695T>C	XP_011524571.1:n.1811-9695T>C
XM_011526270.1:c.1811-9695T>C	XP_011524572.1:n.1811-9695T>C
XM_011526271.1:c.1811-9695T>C	XP_011524573.1:n.1811-9695T>C
XM_011526272.1:c.1811-9695T>C	XP_011524574.1:n.1811-9695T>C
XM_011526273.1:c.1811-9695T>C	XP_011524575.1:n.1811-9695T>C
XM_011526274.1:c.1811-9695T>C	XP_011524576.1:n.1811-9695T>C
XM_011526275.1:c.1811-9695T>C	XP_011524577.1:n.1811-9695T>C
XM_011526276.1:c.1811-9695T>C	XP_011524578.1:n.1811-9695T>C
XM_011526277.1:c.1811-9695T>C	XP_011524579.1:n.1811-9695T>C
XR_935268.1:n.2067-9695T>C
XM_011526269.2:c.1811-9695T>C	XP_011524571.1:n.1811-9695T>C
XM_011526270.3:c.1811-9695T>C	XP_011524572.1:n.1811-9695T>C
XM_011526271.3:c.1811-9695T>C	XP_011524573.1:n.1811-9695T>C
XM_011526273.3:c.1811-9695T>C	XP_011524575.1:n.1811-9695T>C
XM_011526274.3:c.1811-9695T>C	XP_011524576.1:n.1811-9695T>C
XM_011526275.2:c.1811-9695T>C	XP_011524577.1:n.1811-9695T>C
XM_011526276.2:c.1811-9695T>C	XP_011524578.1:n.1811-9695T>C
XM_011526277.2:c.1811-9695T>C	XP_011524579.1:n.1811-9695T>C
XM_017026097.2:c.1811-9695T>C	XP_016881586.1:n.1811-9695T>C
XR_935268.2:n.2067-9695T>C
NM_014643.4:c.1811-9695T>C MANE Select	NP_055458.1:n.1811-9695T>C