Canonical Allele Identifier: CA358896122
Gene: SLC25A4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.186066015T>C (hg19) chr4:g.185144861T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.185144861T>C , CM000666.2:g.185144861T>C GRCh38
NC_000004.11:g.186066015T>C , CM000666.1:g.186066015T>C GRCh37
NC_000004.10:g.186303009T>C NCBI36
NG_013001.1:g.6599T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000281456.11:c.209T>C MANE Select ENSP00000281456.5:p.Phe70Ser
ENST00000281456.10:c.209T>C ENSP00000281456.5:p.Phe70Ser
ENST00000491736.1:c.209T>C ENSP00000476711.1:p.Phe70Ser
NM_001151.3:c.209T>C NP_001142.2:p.Phe70Ser
NM_001151.4:c.209T>C MANE Select NP_001142.2:p.Phe70Ser
Search 100 bp 5'
Search 100 bp 3'