Canonical Allele Identifier: CA2760197281
Gene: MSANTD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.3256765G>A , CM000666.2:g.3256765G>A GRCh38
NC_000004.11:g.3258492G>A , CM000666.1:g.3258492G>A GRCh37
NC_000004.10:g.3228290G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000505599.5:c.729+908G>A ENSP00000425405.1:n.729+908G>A
ENST00000510580.1:c.765+872G>A ENSP00000420966.1:n.765+872G>A
XM_011513464.1:c.729+908G>A XP_011511766.1:n.729+908G>A
XR_924950.1:n.753+908G>A