Canonical Allele Identifier: CA13418617

Gene: MS4A4A

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.60255614C>A , CM000673.2:g.60255614C>A	GRCh38
NC_000011.9:g.60023087C>A , CM000673.1:g.60023087C>A	GRCh37
NC_000011.8:g.59779663C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649552.2:c.60-36611C>A	ENSP00000497952.2:n.60-36611C>A
ENST00000679385.1:c.-24-41583C>A	ENSP00000506313.1:n.-24-41583C>A
ENST00000679553.1:c.60-36611C>A	ENSP00000505712.1:n.60-36611C>A
ENST00000680301.1:c.60-36611C>A	ENSP00000506147.1:n.60-36611C>A
ENST00000680537.1:c.-17+25998C>A	ENSP00000506179.1:n.-17+25998C>A
ENST00000680560.1:c.60-45387C>A	ENSP00000505056.1:n.60-45387C>A
ENST00000680757.1:c.-17+15461C>A	ENSP00000505293.1:n.-17+15461C>A
ENST00000680935.1:c.-17+15461C>A	ENSP00000505050.1:n.-17+15461C>A
ENST00000681288.1:c.60-36611C>A	ENSP00000505714.1:n.60-36611C>A
ENST00000681406.1:c.60-36611C>A	ENSP00000505926.1:n.60-36611C>A