Canonical Allele Identifier: CA938510263
Gene: MS4A5 HGNC NCBI

Linked Data

dbSNP Id: rs2086109974
gnomAD v3: 11-60441263-T-A
gnomAD v4: 11-60441263-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.60441263T>A , CM000673.2:g.60441263T>A GRCh38
NC_000011.9:g.60208736T>A , CM000673.1:g.60208736T>A GRCh37
NC_000011.8:g.59965312T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000300190.7:c.493-6386T>A MANE Select ENSP00000300190.2:n.493-6386T>A
ENST00000300190.6:c.493-6386T>A ENSP00000300190.2:n.493-6386T>A
ENST00000528093.1:c.136-6386T>A
ENST00000528905.1:c.260-6386T>A
ENST00000531403.5:c.*101-6386T>A ENSP00000435192.1:n.*101-6386T>A
ENST00000533885.5:c.*103+5748T>A ENSP00000435330.1:n.*103+5748T>A
NM_023945.2:c.493-6386T>A NP_076434.2:n.493-6386T>A
NM_023945.3:c.493-6386T>A MANE Select NP_076434.2:n.493-6386T>A
Search 100 bp 5'
Search 100 bp 3'