Canonical Allele Identifier: CA11675751
Gene: TNIP2 HGNC NCBI
MyVariant.info:
GRCh38 chr4:g.2743781C>A
GRCh37 chr4:g.2745508C>A
gnomAD v2:
4:2745508 C / A
gnomAD v3:
4:2743781 C / A
gnomAD v4:
chr4-2743781-C-A
Joint Max Group AF 0.63176823 (AMR)
Genomes Max Group AF 0.63176823 (AMR)
dbSNP:
3733223
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.2743781C>A , CM000666.2:g.2743781C>A GRCh38
NC_000004.11:g.2745508C>A , CM000666.1:g.2745508C>A GRCh37
NC_000004.10:g.2715306C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000315423.12:c.1026+606G>T MANE Select ENSP00000321203.7:n.1026+606G>T
ENST00000315423.11:c.1026+606G>T ENSP00000321203.7:n.1026+606G>T
ENST00000502256.1:n.477+606G>T
ENST00000503235.1:c.777+606G>T ENSP00000426314.1:n.777+606G>T
ENST00000505186.1:n.589+606G>T
ENST00000510267.5:c.705+606G>T ENSP00000427613.1:n.705+606G>T
NM_001161527.1:c.705+606G>T NP_001154999.1:n.705+606G>T
NM_001292016.1:c.777+606G>T NP_001278945.1:n.777+606G>T
NM_024309.3:c.1026+606G>T NP_077285.3:n.1026+606G>T
NM_001161527.2:c.705+606G>T NP_001154999.1:n.705+606G>T
NM_001292016.2:c.777+606G>T NP_001278945.1:n.777+606G>T
NM_024309.4:c.1026+606G>T MANE Select NP_077285.3:n.1026+606G>T
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