Canonical Allele Identifier: CA2666513289
Gene: PROK2 HGNC NCBI

Linked Data

gnomAD v4: 3-71784808-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.71784808A>G , CM000665.2:g.71784808A>G GRCh38
NC_000003.11:g.71833959A>G , CM000665.1:g.71833959A>G GRCh37
NC_000003.10:g.71916649A>G NCBI36
NG_008275.1:g.5399T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000295619.4:c.96+149T>C MANE Select ENSP00000295619.3:n.96+149T>C
ENST00000295619.3:c.96+149T>C ENSP00000295619.3:n.96+149T>C
ENST00000353065.7:c.96+149T>C ENSP00000295618.3:n.96+149T>C
NM_001126128.1:c.96+149T>C NP_001119600.1:n.96+149T>C
NM_021935.3:c.96+149T>C NP_068754.1:n.96+149T>C
NM_001126128.2:c.96+149T>C MANE Select NP_001119600.1:n.96+149T>C
NM_021935.4:c.96+149T>C NP_068754.1:n.96+149T>C
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