Canonical Allele Identifier: CA358895909
Gene: SLC25A4 HGNC NCBI

Linked Data

COSMIC: COSM3719076
MyVariant Identifiers: chr4:g.186065924C>G (hg19) chr4:g.185144770C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.185144770C>G , CM000666.2:g.185144770C>G GRCh38
NC_000004.11:g.186065924C>G , CM000666.1:g.186065924C>G GRCh37
NC_000004.10:g.186302918C>G NCBI36
NG_013001.1:g.6508C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000281456.11:c.118C>G MANE Select ENSP00000281456.5:p.His40Asp
ENST00000281456.10:c.118C>G ENSP00000281456.5:p.His40Asp
ENST00000491736.1:c.118C>G ENSP00000476711.1:p.His40Asp
NM_001151.3:c.118C>G NP_001142.2:p.His40Asp
NM_001151.4:c.118C>G MANE Select NP_001142.2:p.His40Asp
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