Canonical Allele Identifier: CA434163195
Gene: PROK2 HGNC NCBI

Linked Data

dbSNP Id: rs1337011837
gnomAD v3: 3-71784972-G-T
gnomAD v4: 3-71784972-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.71784972G>T , CM000665.2:g.71784972G>T GRCh38
NC_000003.11:g.71834123G>T , CM000665.1:g.71834123G>T GRCh37
NC_000003.10:g.71916813G>T NCBI36
NG_008275.1:g.5235C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000295619.4:c.81C>A MANE Select ENSP00000295619.3:p.Ala27=
ENST00000295619.3:c.81C>A ENSP00000295619.3:p.Ala27=
ENST00000353065.7:c.81C>A ENSP00000295618.3:p.Ala27=
NM_001126128.1:c.81C>A NP_001119600.1:p.Ala27=
NM_021935.3:c.81C>A NP_068754.1:p.Ala27=
NM_001126128.2:c.81C>A MANE Select NP_001119600.1:p.Ala27=
NM_021935.4:c.81C>A NP_068754.1:p.Ala27=