Canonical Allele Identifier: CA442866885
Gene: SLC25A4 HGNC NCBI

Linked Data

dbSNP Id: rs1579209519
MyVariant Identifiers: chr4:g.186066106A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.185144952A>G , CM000666.2:g.185144952A>G GRCh38
NC_000004.11:g.186066106A>G , CM000666.1:g.186066106A>G GRCh37
NC_000004.10:g.186303100A>G NCBI36
NG_013001.1:g.6690A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000281456.11:c.300A>G MANE Select ENSP00000281456.5:p.Leu100=
ENST00000281456.10:c.300A>G ENSP00000281456.5:p.Leu100=
ENST00000491736.1:c.300A>G ENSP00000476711.1:p.Leu100=
NM_001151.3:c.300A>G NP_001142.2:p.Leu100=
NM_001151.4:c.300A>G MANE Select NP_001142.2:p.Leu100=