Canonical Allele Identifier: CA408168470
Gene: PROKR2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.5294946G>C (hg19) chr20:g.5314300G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.5314300G>C , CM000682.2:g.5314300G>C GRCh38
NC_000020.10:g.5294946G>C , CM000682.1:g.5294946G>C GRCh37
NC_000020.9:g.5242946G>C NCBI36
NG_008132.1:g.5070C>G
NG_008132.2:g.5070C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000217270.4:c.70C>G ENSP00000217270.3:p.Leu24Val
ENST00000678059.1:c.-22-17C>G ENSP00000503366.1:n.-22-17C>G
ENST00000678254.1:c.70C>G MANE Select ENSP00000504128.1:p.Leu24Val
ENST00000217270.3:c.70C>G ENSP00000217270.3:p.Leu24Val
NM_144773.2:c.70C>G NP_658986.1:p.Leu24Val
XM_005260663.2:c.70C>G XP_005260720.1:p.Leu24Val
XM_011529159.1:c.-22-17C>G XP_011527461.1:n.-22-17C>G
NM_144773.3:c.70C>G NP_658986.1:p.Leu24Val
XM_017027646.1:c.70C>G XP_016883135.1:p.Leu24Val
NM_144773.4:c.70C>G MANE Select NP_658986.1:p.Leu24Val
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