Canonical Allele Identifier: CA1434131108
Gene: MSANTD1 HGNC NCBI

Linked Data

dbSNP Id: rs1578638516

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.3256830T>G , CM000666.2:g.3256830T>G GRCh38
NC_000004.11:g.3258557T>G , CM000666.1:g.3258557T>G GRCh37
NC_000004.10:g.3228355T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000505599.5:c.729+973T>G ENSP00000425405.1:n.729+973T>G
ENST00000510580.1:c.765+937T>G ENSP00000420966.1:n.765+937T>G
XM_011513464.1:c.729+973T>G XP_011511766.1:n.729+973T>G
XR_924950.1:n.753+973T>G