Canonical Allele Identifier: CA2669711260
Gene: MSANTD1 HGNC NCBI

Linked Data

gnomAD v4: 4-3256620-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.3256620T>C , CM000666.2:g.3256620T>C GRCh38
NC_000004.11:g.3258347T>C , CM000666.1:g.3258347T>C GRCh37
NC_000004.10:g.3228145T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000505599.5:c.729+763T>C ENSP00000425405.1:n.729+763T>C
ENST00000510580.1:c.765+727T>C ENSP00000420966.1:n.765+727T>C
XM_011513464.1:c.729+763T>C XP_011511766.1:n.729+763T>C
XR_924950.1:n.753+763T>C
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