Canonical Allele Identifier: CA794017971
Gene: MSANTD1 HGNC NCBI

Linked Data

dbSNP Id: rs1199346383
gnomAD v3: 4-3256777-C-T
gnomAD v4: 4-3256777-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.3256777C>T , CM000666.2:g.3256777C>T GRCh38
NC_000004.11:g.3258504C>T , CM000666.1:g.3258504C>T GRCh37
NC_000004.10:g.3228302C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000505599.5:c.729+920C>T ENSP00000425405.1:n.729+920C>T
ENST00000510580.1:c.765+884C>T ENSP00000420966.1:n.765+884C>T
XM_011513464.1:c.729+920C>T XP_011511766.1:n.729+920C>T
XR_924950.1:n.753+920C>T