Canonical Allele Identifier: CA223271272

Gene: MS4A2

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.60095780C>G , CM000673.2:g.60095780C>G	GRCh38
NC_000011.9:g.59863253C>G , CM000673.1:g.59863253C>G	GRCh37
NC_000011.8:g.59619829C>G	NCBI36
NG_016014.1:g.12117C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278888.8:c.*124C>G MANE Select	ENSP00000278888.3:n.*124C>G
ENST00000278888.7:c.*124C>G	ENSP00000278888.3:n.*124C>G
ENST00000617306.1:c.*124C>G	ENSP00000482594.1:n.*124C>G
NM_000139.4:c.*124C>G	NP_000130.1:n.*124C>G
NM_001256916.1:c.*124C>G	NP_001243845.1:n.*124C>G
XM_005273846.3:c.*124C>G	XP_005273903.1:n.*124C>G
XM_011544850.1:c.*124C>G	XP_011543152.1:n.*124C>G
XM_005273846.4:c.*124C>G	XP_005273903.1:n.*124C>G
XM_011544850.2:c.*124C>G	XP_011543152.1:n.*124C>G
NM_000139.5:c.*124C>G MANE Select	NP_000130.1:n.*124C>G
NM_001256916.2:c.*124C>G	NP_001243845.1:n.*124C>G