Canonical Allele Identifier: CA938510320
Gene: MS4A5 HGNC NCBI

Linked Data

gnomAD v3: 11-60441272-T-G
gnomAD v4: 11-60441272-T-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.60441272T>G , CM000673.2:g.60441272T>G GRCh38
NC_000011.9:g.60208745T>G , CM000673.1:g.60208745T>G GRCh37
NC_000011.8:g.59965321T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000300190.7:c.493-6377T>G MANE Select ENSP00000300190.2:n.493-6377T>G
ENST00000300190.6:c.493-6377T>G ENSP00000300190.2:n.493-6377T>G
ENST00000528093.1:c.136-6377T>G
ENST00000528905.1:c.260-6377T>G
ENST00000531403.5:c.*101-6377T>G ENSP00000435192.1:n.*101-6377T>G
ENST00000533885.5:c.*103+5757T>G ENSP00000435330.1:n.*103+5757T>G
NM_023945.2:c.493-6377T>G NP_076434.2:n.493-6377T>G
NM_023945.3:c.493-6377T>G MANE Select NP_076434.2:n.493-6377T>G
Search 100 bp 5'
Search 100 bp 3'