Canonical Allele Identifier: CA353500958
Gene: PROK2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.71830625G>C (hg19) chr3:g.71781474G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.71781474G>C , CM000665.2:g.71781474G>C GRCh38
NC_000003.11:g.71830625G>C , CM000665.1:g.71830625G>C GRCh37
NC_000003.10:g.71913315G>C NCBI36
NG_008275.1:g.8733C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000295619.4:c.215C>G MANE Select ENSP00000295619.3:p.Thr72Ser
ENST00000295619.3:c.215C>G ENSP00000295619.3:p.Thr72Ser
ENST00000353065.7:c.215C>G ENSP00000295618.3:p.Thr72Ser
NM_001126128.1:c.215C>G NP_001119600.1:p.Thr72Ser
NM_021935.3:c.215C>G NP_068754.1:p.Thr72Ser
XM_017006974.1:c.155C>G XP_016862463.1:p.Thr52Ser
NM_001126128.2:c.215C>G MANE Select NP_001119600.1:p.Thr72Ser
NM_021935.4:c.215C>G NP_068754.1:p.Thr72Ser
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