Canonical Allele Identifier: CA442615219
Gene: SLC25A4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.186066040G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.185144886G>T , CM000666.2:g.185144886G>T GRCh38
NC_000004.11:g.186066040G>T , CM000666.1:g.186066040G>T GRCh37
NC_000004.10:g.186303034G>T NCBI36
NG_013001.1:g.6624G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000281456.11:c.234G>T MANE Select ENSP00000281456.5:p.Val78=
ENST00000281456.10:c.234G>T ENSP00000281456.5:p.Val78=
ENST00000491736.1:c.234G>T ENSP00000476711.1:p.Val78=
NM_001151.3:c.234G>T NP_001142.2:p.Val78=
NM_001151.4:c.234G>T MANE Select NP_001142.2:p.Val78=
Search 100 bp 5'
Search 100 bp 3'