Canonical Allele Identifier: CA1058634270
Gene: MSANTD1 HGNC NCBI

Linked Data

dbSNP Id: rs1722406637
gnomAD v3: 4-3256735-G-A
gnomAD v4: 4-3256735-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.3256735G>A , CM000666.2:g.3256735G>A GRCh38
NC_000004.11:g.3258462G>A , CM000666.1:g.3258462G>A GRCh37
NC_000004.10:g.3228260G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000505599.5:c.729+878G>A ENSP00000425405.1:n.729+878G>A
ENST00000510580.1:c.765+842G>A ENSP00000420966.1:n.765+842G>A
XM_011513464.1:c.729+878G>A XP_011511766.1:n.729+878G>A
XR_924950.1:n.753+878G>A