Canonical Allele Identifier: CA76548126
Gene: PROK2 HGNC NCBI

Linked Data

dbSNP Id: rs932800598
MyVariant Identifiers: chr3:g.71833935C>T (hg19) chr3:g.71784784C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.71784784C>T , CM000665.2:g.71784784C>T GRCh38
NC_000003.11:g.71833935C>T , CM000665.1:g.71833935C>T GRCh37
NC_000003.10:g.71916625C>T NCBI36
NG_008275.1:g.5423G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000295619.4:c.96+173G>A MANE Select ENSP00000295619.3:n.96+173G>A
ENST00000295619.3:c.96+173G>A ENSP00000295619.3:n.96+173G>A
ENST00000353065.7:c.96+173G>A ENSP00000295618.3:n.96+173G>A
NM_001126128.1:c.96+173G>A NP_001119600.1:n.96+173G>A
NM_021935.3:c.96+173G>A NP_068754.1:n.96+173G>A
NM_001126128.2:c.96+173G>A MANE Select NP_001119600.1:n.96+173G>A
NM_021935.4:c.96+173G>A NP_068754.1:n.96+173G>A
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