Canonical Allele Identifier: CA91448504
Gene: MSANTD1 HGNC NCBI

Linked Data

dbSNP Id: rs540190505
gnomAD v3: 4-3256639-T-C
gnomAD v4: 4-3256639-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.3256639T>C , CM000666.2:g.3256639T>C GRCh38
NC_000004.11:g.3258366T>C , CM000666.1:g.3258366T>C GRCh37
NC_000004.10:g.3228164T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000505599.5:c.729+782T>C ENSP00000425405.1:n.729+782T>C
ENST00000510580.1:c.765+746T>C ENSP00000420966.1:n.765+746T>C
XM_011513464.1:c.729+782T>C XP_011511766.1:n.729+782T>C
XR_924950.1:n.753+782T>C