Canonical Allele Identifier: CA174543

Gene: ZNF184

Linked Data

• ClinVar Variation Id: 161657
• ClinVar RCV Id: RCV000149193
• dbSNP Id: rs193921063
• COSMIC: COSM1178203
• MyVariant Identifiers: chr6:g.27425151G>T (hg19) ; chr6:g.27457372G>T (hg38)
• PubMed: PMID:23265383

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.27457372G>T , CM000668.2:g.27457372G>T	GRCh38
NC_000006.11:g.27425151G>T , CM000668.1:g.27425151G>T	GRCh37
NC_000006.10:g.27533130G>T	NCBI36
NG_052614.1:g.20747C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683788.1:c.113C>A MANE Select	ENSP00000508298.1:p.Thr38Asn
ENST00000211936.10:c.113C>A	ENSP00000211936.6:p.Thr38Asn
ENST00000377419.1:c.113C>A	ENSP00000366636.1:p.Thr38Asn
NM_007149.2:c.113C>A	NP_009080.2:p.Thr38Asn
XM_005249379.2:c.113C>A	XP_005249436.1:p.Thr38Asn
XM_005249380.2:c.113C>A	XP_005249437.1:p.Thr38Asn
XM_011514860.1:c.-145C>A	XP_011513162.1:n.-145C>A
XM_011514861.1:c.-145C>A	XP_011513163.1:n.-145C>A
NM_001318891.1:c.113C>A	NP_001305820.1:p.Thr38Asn
NM_001318892.1:c.113C>A	NP_001305821.1:p.Thr38Asn
NM_001318893.1:c.-145C>A	NP_001305822.1:n.-145C>A
NM_001347832.1:c.-145C>A	NP_001334761.1:n.-145C>A
NR_144687.1:n.398C>A
NR_144688.1:n.398C>A
NM_001318893.2:c.-145C>A	NP_001305822.1:n.-145C>A
NM_001347832.2:c.-145C>A	NP_001334761.1:n.-145C>A
NR_144687.2:n.385C>A
NR_144688.2:n.385C>A
NM_001318891.2:c.113C>A MANE Select	NP_001305820.1:p.Thr38Asn
NM_001318892.2:c.113C>A	NP_001305821.1:p.Thr38Asn
NM_007149.3:c.113C>A	NP_009080.2:p.Thr38Asn