Canonical Allele Identifier: CA12501531
Gene: HOXA10 HGNC NCBI
HOXA9 HGNC NCBI
MyVariant.info:
GRCh38 chr7:g.27174938T>C
GRCh37 chr7:g.27214557T>C
gnomAD v2:
7:27214557 T / C
gnomAD v3:
7:27174938 T / C
gnomAD v4:
chr7-27174938-T-C
Joint Max Group AF 0.49361983 (AMR)
Genomes Max Group AF 0.493416 (AMR)
Exomes Max Group AF 0.41272541 (AMR)
dbSNP:
3779456
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27174938T>C , CM000669.2:g.27174938T>C GRCh38
NC_000007.13:g.27214557T>C , CM000669.1:g.27214557T>C GRCh37
NC_000007.12:g.27181082T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000396344.4:c.11-2765A>G (HOXA10) ENSP00000379633.4:n.11-2765A>G
ENST00000465941.1:n.243A>G (HOXA9)
ENST00000470747.4:c.10+4708A>G ENSP00000421799.3:n.10+4708A>G
NR_037939.1:n.617-2765A>G (HOXA10)
NR_037940.1:n.616+4708A>G
NR_037939.2:n.217-2765A>G (HOXA10)
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