Canonical Allele Identifier: CA1434131159
Gene: MSANTD1 HGNC NCBI

Linked Data

dbSNP Id: rs1722411073

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.3256943C>G , CM000666.2:g.3256943C>G GRCh38
NC_000004.11:g.3258670C>G , CM000666.1:g.3258670C>G GRCh37
NC_000004.10:g.3228468C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000505599.5:c.729+1086C>G ENSP00000425405.1:n.729+1086C>G
ENST00000510580.1:c.765+1050C>G ENSP00000420966.1:n.765+1050C>G
XM_011513464.1:c.729+1086C>G XP_011511766.1:n.729+1086C>G
XR_924950.1:n.753+1086C>G