Canonical Allele Identifier: CA2705000935

Gene: MSANTD1

Linked Data

• dbSNP Id: rs2110325130

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.3256802G>C , CM000666.2:g.3256802G>C	GRCh38
NC_000004.11:g.3258529G>C , CM000666.1:g.3258529G>C	GRCh37
NC_000004.10:g.3228327G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505599.5:c.729+945G>C	ENSP00000425405.1:n.729+945G>C
ENST00000510580.1:c.765+909G>C	ENSP00000420966.1:n.765+909G>C
XM_011513464.1:c.729+945G>C	XP_011511766.1:n.729+945G>C
XR_924950.1:n.753+945G>C