Canonical Allele Identifier: CA9754441
Gene: PROKR2 HGNC NCBI

Linked Data

dbSNP Id: rs375646689
gnomAD v2: 20-5294944-G-C
gnomAD v4: 20-5314298-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.5314298G>C , CM000682.2:g.5314298G>C GRCh38
NC_000020.10:g.5294944G>C , CM000682.1:g.5294944G>C GRCh37
NC_000020.9:g.5242944G>C NCBI36
NG_008132.1:g.5072C>G
NG_008132.2:g.5072C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000217270.4:c.72C>G ENSP00000217270.3:p.Leu24=
ENST00000678059.1:c.-22-15C>G ENSP00000503366.1:n.-22-15C>G
ENST00000678254.1:c.72C>G MANE Select ENSP00000504128.1:p.Leu24=
ENST00000217270.3:c.72C>G ENSP00000217270.3:p.Leu24=
NM_144773.2:c.72C>G NP_658986.1:p.Leu24=
XM_005260663.2:c.72C>G XP_005260720.1:p.Leu24=
XM_011529159.1:c.-22-15C>G XP_011527461.1:n.-22-15C>G
NM_144773.3:c.72C>G NP_658986.1:p.Leu24=
XM_017027646.1:c.72C>G XP_016883135.1:p.Leu24=
NM_144773.4:c.72C>G MANE Select NP_658986.1:p.Leu24=