Canonical Allele Identifier: CA2666513298
Gene: PROK2 HGNC NCBI

Linked Data

dbSNP Id: rs2108199916
gnomAD v4: 3-71784813-A-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.71784813A>G , CM000665.2:g.71784813A>G GRCh38
NC_000003.11:g.71833964A>G , CM000665.1:g.71833964A>G GRCh37
NC_000003.10:g.71916654A>G NCBI36
NG_008275.1:g.5394T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000295619.4:c.96+144T>C MANE Select ENSP00000295619.3:n.96+144T>C
ENST00000295619.3:c.96+144T>C ENSP00000295619.3:n.96+144T>C
ENST00000353065.7:c.96+144T>C ENSP00000295618.3:n.96+144T>C
NM_001126128.1:c.96+144T>C NP_001119600.1:n.96+144T>C
NM_021935.3:c.96+144T>C NP_068754.1:n.96+144T>C
NM_001126128.2:c.96+144T>C MANE Select NP_001119600.1:n.96+144T>C
NM_021935.4:c.96+144T>C NP_068754.1:n.96+144T>C
Search 100 bp 5'
Search 100 bp 3'