Canonical Allele Identifier: CA353501236
Gene: PROK2 HGNC NCBI

Linked Data

dbSNP Id: rs104893767
gnomAD v4: 3-71784959-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.71784959C>T , CM000665.2:g.71784959C>T GRCh38
NC_000003.11:g.71834110C>T , CM000665.1:g.71834110C>T GRCh37
NC_000003.10:g.71916800C>T NCBI36
NG_008275.1:g.5248G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000295619.4:c.94G>A MANE Select ENSP00000295619.3:p.Gly32Arg
ENST00000295619.3:c.94G>A ENSP00000295619.3:p.Gly32Arg
ENST00000353065.7:c.94G>A ENSP00000295618.3:p.Gly32Arg
NM_001126128.1:c.94G>A NP_001119600.1:p.Gly32Arg
NM_021935.3:c.94G>A NP_068754.1:p.Gly32Arg
NM_001126128.2:c.94G>A MANE Select NP_001119600.1:p.Gly32Arg
NM_021935.4:c.94G>A NP_068754.1:p.Gly32Arg