Canonical Allele Identifier: CA13024097
Gene: RLN2 HGNC NCBI
RLN1 HGNC NCBI
MyVariant.info:
GRCh38 chr9:g.5306824A>G
GRCh37 chr9:g.5306824A>G
gnomAD v2:
9:5306824 A / G
gnomAD v3:
9:5306824 A / G
gnomAD v4:
chr9-5306824-A-G
Joint Max Group AF 0.27689046 (AFR)
Genomes Max Group AF 0.27689046 (AFR)
dbSNP:
3758239
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.5306824A>G , CM000671.2:g.5306824A>G GRCh38
NC_000009.11:g.5306824A>G , CM000671.1:g.5306824A>G GRCh37
NC_000009.10:g.5296824A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011518003.1:c.-63+554T>C (RLN2) XP_011516305.1:n.-63+554T>C
XM_024447637.1:c.-63+554T>C (RLN1) XP_024303405.1:n.-63+554T>C
XM_024447646.1:c.-63+554T>C (RLN2) XP_024303414.1:n.-63+554T>C
XM_024447647.1:c.-63+554T>C (RLN2) XP_024303415.1:n.-63+554T>C
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