Canonical Allele Identifier: CA749456823
Gene: RIPK4 HGNC NCBI

Linked Data

dbSNP Id: rs1330153884
gnomAD v3: 21-41757053-T-C
gnomAD v4: 21-41757053-T-C
MyVariant Identifiers: chr21:g.43177213T>C (hg19) chr21:g.41757053T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.41757053T>C , CM000683.2:g.41757053T>C GRCh38
NC_000021.8:g.43177213T>C , CM000683.1:g.43177213T>C GRCh37
NC_000021.7:g.42050282T>C NCBI36
NG_032113.1:g.15037A>G
NG_032113.2:g.15037A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000332512.8:c.183-237A>G MANE Select ENSP00000332454.3:n.183-237A>G
ENST00000332512.7:c.183-237A>G ENSP00000332454.3:n.183-237A>G
ENST00000352483.3:c.183-237A>G ENSP00000330161.2:n.183-237A>G
NM_020639.2:c.183-237A>G NP_065690.2:n.183-237A>G
NM_020639.3:c.183-237A>G MANE Select NP_065690.2:n.183-237A>G
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