Canonical Allele Identifier: CA91448563
Gene: MSANTD1 HGNC NCBI

Linked Data

dbSNP Id: rs1005479456
gnomAD v3: 4-3256720-A-G
gnomAD v4: 4-3256720-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.3256720A>G , CM000666.2:g.3256720A>G GRCh38
NC_000004.11:g.3258447A>G , CM000666.1:g.3258447A>G GRCh37
NC_000004.10:g.3228245A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000505599.5:c.729+863A>G ENSP00000425405.1:n.729+863A>G
ENST00000510580.1:c.765+827A>G ENSP00000420966.1:n.765+827A>G
XM_011513464.1:c.729+863A>G XP_011511766.1:n.729+863A>G
XR_924950.1:n.753+863A>G