Canonical Allele Identifier: CA2702958910
Gene: PROK2 HGNC NCBI

Linked Data

dbSNP Id: rs2050198311
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.71784773G>A , CM000665.2:g.71784773G>A GRCh38
NC_000003.11:g.71833924G>A , CM000665.1:g.71833924G>A GRCh37
NC_000003.10:g.71916614G>A NCBI36
NG_008275.1:g.5434C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000295619.4:c.96+184C>T MANE Select ENSP00000295619.3:n.96+184C>T
ENST00000295619.3:c.96+184C>T ENSP00000295619.3:n.96+184C>T
ENST00000353065.7:c.96+184C>T ENSP00000295618.3:n.96+184C>T
NM_001126128.1:c.96+184C>T NP_001119600.1:n.96+184C>T
NM_021935.3:c.96+184C>T NP_068754.1:n.96+184C>T
NM_001126128.2:c.96+184C>T MANE Select NP_001119600.1:n.96+184C>T
NM_021935.4:c.96+184C>T NP_068754.1:n.96+184C>T
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