Canonical Allele Identifier: CA794017954
Gene: MSANTD1 HGNC NCBI

Linked Data

dbSNP Id: rs1250794701
gnomAD v3: 4-3256740-T-G
gnomAD v4: 4-3256740-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.3256740T>G , CM000666.2:g.3256740T>G GRCh38
NC_000004.11:g.3258467T>G , CM000666.1:g.3258467T>G GRCh37
NC_000004.10:g.3228265T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000505599.5:c.729+883T>G ENSP00000425405.1:n.729+883T>G
ENST00000510580.1:c.765+847T>G ENSP00000420966.1:n.765+847T>G
XM_011513464.1:c.729+883T>G XP_011511766.1:n.729+883T>G
XR_924950.1:n.753+883T>G