Canonical Allele Identifier: CA15205752
Gene:
MyVariant.info:
GRCh38 chr2:g.644953A>G
GRCh37 chr2:g.644953A>G
gnomAD v2:
2:644953 A / G
gnomAD v3:
2:644953 A / G
gnomAD v4:
chr2-644953-A-G
Joint Max Group AF 0.89678891 (EAS)
Genomes Max Group AF 0.89678891 (EAS)
dbSNP:
7561317
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.644953A>G , CM000664.2:g.644953A>G GRCh38
NC_000002.11:g.644953A>G , CM000664.1:g.644953A>G GRCh37
NC_000002.10:g.634953A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011510438.1:c.*573-960A>G XP_011508740.1:n.*573-960A>G
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