Canonical Allele Identifier: CA1976770740
Gene: MS4A4A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.60197519G>C , CM000673.2:g.60197519G>C GRCh38
NC_000011.9:g.59964992G>C , CM000673.1:g.59964992G>C GRCh37
NC_000011.8:g.59721568G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000649552.2:c.59+11348G>C ENSP00000497952.2:n.59+11348G>C
ENST00000679385.1:c.-25+11348G>C ENSP00000506313.1:n.-25+11348G>C
ENST00000679553.1:c.59+11348G>C ENSP00000505712.1:n.59+11348G>C
ENST00000680301.1:c.59+11348G>C ENSP00000506147.1:n.59+11348G>C
ENST00000680537.1:c.-176+11348G>C ENSP00000506179.1:n.-176+11348G>C
ENST00000680560.1:c.59+11348G>C ENSP00000505056.1:n.59+11348G>C
ENST00000680757.1:c.-105+11348G>C ENSP00000505293.1:n.-105+11348G>C
ENST00000680935.1:c.-105+11348G>C ENSP00000505050.1:n.-105+11348G>C
ENST00000681288.1:c.59+11348G>C ENSP00000505714.1:n.59+11348G>C
ENST00000681406.1:c.59+11348G>C ENSP00000505926.1:n.59+11348G>C