Canonical Allele Identifier: CA1058634268
Gene: MSANTD1 HGNC NCBI

Linked Data

dbSNP Id: rs1722406519
gnomAD v3: 4-3256731-T-C
gnomAD v4: 4-3256731-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.3256731T>C , CM000666.2:g.3256731T>C GRCh38
NC_000004.11:g.3258458T>C , CM000666.1:g.3258458T>C GRCh37
NC_000004.10:g.3228256T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000505599.5:c.729+874T>C ENSP00000425405.1:n.729+874T>C
ENST00000510580.1:c.765+838T>C ENSP00000420966.1:n.765+838T>C
XM_011513464.1:c.729+874T>C XP_011511766.1:n.729+874T>C
XR_924950.1:n.753+874T>C