Canonical Allele Identifier: CA2669711281
Gene: MSANTD1 HGNC NCBI

Linked Data

gnomAD v4: 4-3256642-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.3256642A>G , CM000666.2:g.3256642A>G GRCh38
NC_000004.11:g.3258369A>G , CM000666.1:g.3258369A>G GRCh37
NC_000004.10:g.3228167A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000505599.5:c.729+785A>G ENSP00000425405.1:n.729+785A>G
ENST00000510580.1:c.765+749A>G ENSP00000420966.1:n.765+749A>G
XM_011513464.1:c.729+785A>G XP_011511766.1:n.729+785A>G
XR_924950.1:n.753+785A>G