Canonical Allele Identifier: CA2669711337
Gene: MSANTD1 HGNC NCBI

Linked Data

gnomAD v4: 4-3256725-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.3256725A>G , CM000666.2:g.3256725A>G GRCh38
NC_000004.11:g.3258452A>G , CM000666.1:g.3258452A>G GRCh37
NC_000004.10:g.3228250A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000505599.5:c.729+868A>G ENSP00000425405.1:n.729+868A>G
ENST00000510580.1:c.765+832A>G ENSP00000420966.1:n.765+832A>G
XM_011513464.1:c.729+868A>G XP_011511766.1:n.729+868A>G
XR_924950.1:n.753+868A>G