Canonical Allele Identifier: CA2669711313

Gene: MSANTD1

Linked Data

• gnomAD v4: 4-3256685-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.3256685T>C , CM000666.2:g.3256685T>C	GRCh38
NC_000004.11:g.3258412T>C , CM000666.1:g.3258412T>C	GRCh37
NC_000004.10:g.3228210T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505599.5:c.729+828T>C	ENSP00000425405.1:n.729+828T>C
ENST00000510580.1:c.765+792T>C	ENSP00000420966.1:n.765+792T>C
XM_011513464.1:c.729+828T>C	XP_011511766.1:n.729+828T>C
XR_924950.1:n.753+828T>C