Canonical Allele Identifier: CA91448566

Gene: MSANTD1

Linked Data

• dbSNP Id: rs1018164287
• gnomAD v3: 4-3256723-G-A
• gnomAD v4: 4-3256723-G-A
• MyVariant Identifiers: chr4:g.3258450G>A (hg19) ; chr4:g.3256723G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.3256723G>A , CM000666.2:g.3256723G>A	GRCh38
NC_000004.11:g.3258450G>A , CM000666.1:g.3258450G>A	GRCh37
NC_000004.10:g.3228248G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000505599.5:c.729+866G>A	ENSP00000425405.1:n.729+866G>A
ENST00000510580.1:c.765+830G>A	ENSP00000420966.1:n.765+830G>A
XM_011513464.1:c.729+866G>A	XP_011511766.1:n.729+866G>A
XR_924950.1:n.753+866G>A