Canonical Allele Identifier: CA353501255
Gene: PROK2 HGNC NCBI

Linked Data

gnomAD v4: 3-71784968-C-G
MyVariant Identifiers: chr3:g.71834119C>G (hg19) chr3:g.71784968C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.71784968C>G , CM000665.2:g.71784968C>G GRCh38
NC_000003.11:g.71834119C>G , CM000665.1:g.71834119C>G GRCh37
NC_000003.10:g.71916809C>G NCBI36
NG_008275.1:g.5239G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000295619.4:c.85G>C MANE Select ENSP00000295619.3:p.Val29Leu
ENST00000295619.3:c.85G>C ENSP00000295619.3:p.Val29Leu
ENST00000353065.7:c.85G>C ENSP00000295618.3:p.Val29Leu
NM_001126128.1:c.85G>C NP_001119600.1:p.Val29Leu
NM_021935.3:c.85G>C NP_068754.1:p.Val29Leu
NM_001126128.2:c.85G>C MANE Select NP_001119600.1:p.Val29Leu
NM_021935.4:c.85G>C NP_068754.1:p.Val29Leu
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