Canonical Allele Identifier: CA11632806
Gene: MSANTD1 HGNC NCBI
MyVariant.info:
GRCh38 chr4:g.3256646A>G
GRCh37 chr4:g.3258373A>G
gnomAD v2:
4:3258373 A / G
gnomAD v3:
4:3256646 A / G
gnomAD v4:
chr4-3256646-A-G
Joint Max Group AF 0.36289598 (NFE)
Genomes Max Group AF 0.36304071 (NFE)
Exomes Max Group AF 0.16164132 (NFE)
dbSNP:
1006798
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.3256646A>G , CM000666.2:g.3256646A>G GRCh38
NC_000004.11:g.3258373A>G , CM000666.1:g.3258373A>G GRCh37
NC_000004.10:g.3228171A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000505599.5:c.729+789A>G ENSP00000425405.1:n.729+789A>G
ENST00000510580.1:c.765+753A>G ENSP00000420966.1:n.765+753A>G
XM_011513464.1:c.729+789A>G XP_011511766.1:n.729+789A>G
XR_924950.1:n.753+789A>G
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