Canonical Allele Identifier: CA1434131051
Gene: MSANTD1 HGNC NCBI

Linked Data

dbSNP Id: rs1722406152
gnomAD v4: 4-3256712-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.3256712G>A , CM000666.2:g.3256712G>A GRCh38
NC_000004.11:g.3258439G>A , CM000666.1:g.3258439G>A GRCh37
NC_000004.10:g.3228237G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000505599.5:c.729+855G>A ENSP00000425405.1:n.729+855G>A
ENST00000510580.1:c.765+819G>A ENSP00000420966.1:n.765+819G>A
XM_011513464.1:c.729+855G>A XP_011511766.1:n.729+855G>A
XR_924950.1:n.753+855G>A