Canonical Allele Identifier: CA240497922
Gene: PAWR HGNC NCBI

Linked Data

dbSNP Id: rs8176874

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.79620593T>C , CM000674.2:g.79620593T>C GRCh38
NC_000012.11:g.80014373T>C , CM000674.1:g.80014373T>C GRCh37
NC_000012.10:g.78538504T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000328827.9:c.648+483A>G MANE Select ENSP00000328088.4:n.648+483A>G
ENST00000328827.8:c.648+483A>G ENSP00000328088.4:n.648+483A>G
ENST00000549050.1:n.57+11513A>G
ENST00000551712.1:c.484+483A>G
NM_002583.2:c.648+483A>G NP_002574.2:n.648+483A>G
XM_006719435.2:c.648+483A>G XP_006719498.1:n.648+483A>G
XM_006719436.2:c.648+483A>G XP_006719499.1:n.648+483A>G
NM_001354732.1:c.648+483A>G NP_001341661.1:n.648+483A>G
NM_001354733.1:c.648+483A>G NP_001341662.1:n.648+483A>G
NM_002583.3:c.648+483A>G NP_002574.2:n.648+483A>G
XM_017019378.1:c.648+483A>G XP_016874867.1:n.648+483A>G
NM_002583.4:c.648+483A>G MANE Select NP_002574.2:n.648+483A>G
NM_001354732.2:c.648+483A>G NP_001341661.1:n.648+483A>G
NM_001354733.2:c.648+483A>G NP_001341662.1:n.648+483A>G