Canonical Allele Identifier: CA678877845
Gene: MS4A5 HGNC NCBI

Linked Data

dbSNP Id: rs1204013771
MyVariant Identifiers: chr11:g.60208734A>G (hg19) chr11:g.60441261A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.60441261A>G , CM000673.2:g.60441261A>G GRCh38
NC_000011.9:g.60208734A>G , CM000673.1:g.60208734A>G GRCh37
NC_000011.8:g.59965310A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000300190.7:c.493-6388A>G MANE Select ENSP00000300190.2:n.493-6388A>G
ENST00000300190.6:c.493-6388A>G ENSP00000300190.2:n.493-6388A>G
ENST00000528093.1:c.136-6388A>G
ENST00000528905.1:c.260-6388A>G
ENST00000531403.5:c.*101-6388A>G ENSP00000435192.1:n.*101-6388A>G
ENST00000533885.5:c.*103+5746A>G ENSP00000435330.1:n.*103+5746A>G
NM_023945.2:c.493-6388A>G NP_076434.2:n.493-6388A>G
NM_023945.3:c.493-6388A>G MANE Select NP_076434.2:n.493-6388A>G
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