Canonical Allele Identifier: CA2702958914
Gene: PROK2 HGNC NCBI

Linked Data

dbSNP Id: rs2050198358
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.71784774C>A , CM000665.2:g.71784774C>A GRCh38
NC_000003.11:g.71833925C>A , CM000665.1:g.71833925C>A GRCh37
NC_000003.10:g.71916615C>A NCBI36
NG_008275.1:g.5433G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000295619.4:c.96+183G>T MANE Select ENSP00000295619.3:n.96+183G>T
ENST00000295619.3:c.96+183G>T ENSP00000295619.3:n.96+183G>T
ENST00000353065.7:c.96+183G>T ENSP00000295618.3:n.96+183G>T
NM_001126128.1:c.96+183G>T NP_001119600.1:n.96+183G>T
NM_021935.3:c.96+183G>T NP_068754.1:n.96+183G>T
NM_001126128.2:c.96+183G>T MANE Select NP_001119600.1:n.96+183G>T
NM_021935.4:c.96+183G>T NP_068754.1:n.96+183G>T
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