Canonical Allele Identifier: CA749456788
Gene: RIPK4 HGNC NCBI

Linked Data

dbSNP Id: rs1432376776
gnomAD v3: 21-41756959-C-T
gnomAD v4: 21-41756959-C-T
MyVariant Identifiers: chr21:g.43177119C>T (hg19) chr21:g.41756959C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.41756959C>T , CM000683.2:g.41756959C>T GRCh38
NC_000021.8:g.43177119C>T , CM000683.1:g.43177119C>T GRCh37
NC_000021.7:g.42050188C>T NCBI36
NG_032113.1:g.15131G>A
NG_032113.2:g.15131G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000332512.8:c.183-143G>A MANE Select ENSP00000332454.3:n.183-143G>A
ENST00000332512.7:c.183-143G>A ENSP00000332454.3:n.183-143G>A
ENST00000352483.3:c.183-143G>A ENSP00000330161.2:n.183-143G>A
NM_020639.2:c.183-143G>A NP_065690.2:n.183-143G>A
NM_020639.3:c.183-143G>A MANE Select NP_065690.2:n.183-143G>A
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