Canonical Allele Identifier: CA91448559
Gene: MSANTD1 HGNC NCBI

Linked Data

dbSNP Id: rs888433635

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.3256714G>T , CM000666.2:g.3256714G>T GRCh38
NC_000004.11:g.3258441G>T , CM000666.1:g.3258441G>T GRCh37
NC_000004.10:g.3228239G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000505599.5:c.729+857G>T ENSP00000425405.1:n.729+857G>T
ENST00000510580.1:c.765+821G>T ENSP00000420966.1:n.765+821G>T
XM_011513464.1:c.729+857G>T XP_011511766.1:n.729+857G>T
XR_924950.1:n.753+857G>T