Canonical Allele Identifier: CA410325801
Gene: RIPK4 HGNC NCBI

Linked Data

dbSNP Id: rs2061151862
gnomAD v3: 21-41741154-T-C
gnomAD v4: 21-41741154-T-C
MyVariant Identifiers: chr21:g.43161314T>C (hg19) chr21:g.41741154T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.41741154T>C , CM000683.2:g.41741154T>C GRCh38
NC_000021.8:g.43161314T>C , CM000683.1:g.43161314T>C GRCh37
NC_000021.7:g.42034383T>C NCBI36
NG_032113.1:g.30936A>G
NG_032113.2:g.30936A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000332512.8:c.2039A>G MANE Select ENSP00000332454.3:p.Asn680Ser
ENST00000332512.7:c.2039A>G ENSP00000332454.3:p.Asn680Ser
ENST00000352483.3:c.2183A>G ENSP00000330161.2:p.Asn728Ser
NM_020639.2:c.2039A>G NP_065690.2:p.Asn680Ser
NM_020639.3:c.2039A>G MANE Select NP_065690.2:p.Asn680Ser
Search 100 bp 5'
Search 100 bp 3'