Canonical Allele Identifier: CA91448692
Gene: MSANTD1 HGNC NCBI

Linked Data

dbSNP Id: rs539848448
gnomAD v3: 4-3256854-A-G
gnomAD v4: 4-3256854-A-G
MyVariant Identifiers: chr4:g.3258581A>G (hg19) chr4:g.3256854A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.3256854A>G , CM000666.2:g.3256854A>G GRCh38
NC_000004.11:g.3258581A>G , CM000666.1:g.3258581A>G GRCh37
NC_000004.10:g.3228379A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000505599.5:c.729+997A>G ENSP00000425405.1:n.729+997A>G
ENST00000510580.1:c.765+961A>G ENSP00000420966.1:n.765+961A>G
XM_011513464.1:c.729+997A>G XP_011511766.1:n.729+997A>G
XR_924950.1:n.753+997A>G
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