Canonical Allele Identifier: CA76548182
Gene: PROK2 HGNC NCBI

Linked Data

dbSNP Id: rs371322046
gnomAD v2: 3-71834019-T-C
gnomAD v3: 3-71784868-T-C
gnomAD v4: 3-71784868-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.71784868T>C , CM000665.2:g.71784868T>C GRCh38
NC_000003.11:g.71834019T>C , CM000665.1:g.71834019T>C GRCh37
NC_000003.10:g.71916709T>C NCBI36
NG_008275.1:g.5339A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000295619.4:c.96+89A>G MANE Select ENSP00000295619.3:n.96+89A>G
ENST00000295619.3:c.96+89A>G ENSP00000295619.3:n.96+89A>G
ENST00000353065.7:c.96+89A>G ENSP00000295618.3:n.96+89A>G
NM_001126128.1:c.96+89A>G NP_001119600.1:n.96+89A>G
NM_021935.3:c.96+89A>G NP_068754.1:n.96+89A>G
NM_001126128.2:c.96+89A>G MANE Select NP_001119600.1:n.96+89A>G
NM_021935.4:c.96+89A>G NP_068754.1:n.96+89A>G