Canonical Allele Identifier: CA13553722
Gene: MRGPRX9P HGNC NCBI
MyVariant.info:
GRCh38 chr11:g.19030325T>C
GRCh37 chr11:g.19051872T>C
gnomAD v2:
11:19051872 T / C
gnomAD v3:
11:19030325 T / C
gnomAD v4:
chr11-19030325-T-C
Joint Max Group AF 0.19243953 (EAS)
Genomes Max Group AF 0.19232542 (EAS)
Exomes Max Group AF 0.05475465 (NFE)
dbSNP:
7111562
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.19030325T>C , CM000673.2:g.19030325T>C GRCh38
NC_000011.9:g.19051872T>C , CM000673.1:g.19051872T>C GRCh37
NC_000011.8:g.19008448T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000532323.1:n.114A>G
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