Canonical Allele Identifier: CA2666513504
Gene: PROK2 HGNC NCBI

Linked Data

gnomAD v4: 3-71784951-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.71784951G>C , CM000665.2:g.71784951G>C GRCh38
NC_000003.11:g.71834102G>C , CM000665.1:g.71834102G>C GRCh37
NC_000003.10:g.71916792G>C NCBI36
NG_008275.1:g.5256C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000295619.4:c.96+6C>G MANE Select ENSP00000295619.3:n.96+6C>G
ENST00000295619.3:c.96+6C>G ENSP00000295619.3:n.96+6C>G
ENST00000353065.7:c.96+6C>G ENSP00000295618.3:n.96+6C>G
NM_001126128.1:c.96+6C>G NP_001119600.1:n.96+6C>G
NM_021935.3:c.96+6C>G NP_068754.1:n.96+6C>G
NM_001126128.2:c.96+6C>G MANE Select NP_001119600.1:n.96+6C>G
NM_021935.4:c.96+6C>G NP_068754.1:n.96+6C>G
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