Canonical Allele Identifier: CA442614935
Gene: SLC25A4 HGNC NCBI

Linked Data

dbSNP Id: rs1579208807
MyVariant Identifiers: chr4:g.186064610C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.185143456C>G , CM000666.2:g.185143456C>G GRCh38
NC_000004.11:g.186064610C>G , CM000666.1:g.186064610C>G GRCh37
NC_000004.10:g.186301604C>G NCBI36
NG_013001.1:g.5194C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000281456.11:c.84C>G MANE Select ENSP00000281456.5:p.Pro28=
ENST00000281456.10:c.84C>G ENSP00000281456.5:p.Pro28=
ENST00000491736.1:c.84C>G ENSP00000476711.1:p.Pro28=
NM_001151.3:c.84C>G NP_001142.2:p.Pro28=
NM_001151.4:c.84C>G MANE Select NP_001142.2:p.Pro28=
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