Canonical Allele Identifier: CA2492031
Gene: PROK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 379292
ClinVar RCV Id: RCV000438787
dbSNP Id: rs571314719
gnomAD v2: 3-71834238-T-C
gnomAD v3: 3-71785087-T-C
gnomAD v4: 3-71785087-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.71785087T>C , CM000665.2:g.71785087T>C GRCh38
NC_000003.11:g.71834238T>C , CM000665.1:g.71834238T>C GRCh37
NC_000003.10:g.71916928T>C NCBI36
NG_008275.1:g.5120A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000295619.4:c.-35A>G MANE Select ENSP00000295619.3:n.-35A>G
ENST00000353065.7:c.-35A>G ENSP00000295618.3:n.-35A>G
NM_001126128.1:c.-35A>G NP_001119600.1:n.-35A>G
NM_021935.3:c.-35A>G NP_068754.1:n.-35A>G
NM_001126128.2:c.-35A>G MANE Select NP_001119600.1:n.-35A>G
NM_021935.4:c.-35A>G NP_068754.1:n.-35A>G