Canonical Allele Identifier: CA358896169
Gene: SLC25A4 HGNC NCBI

Linked Data

gnomAD v4: 4-185144882-A-G
MyVariant Identifiers: chr4:g.186066036A>G (hg19) chr4:g.185144882A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.185144882A>G , CM000666.2:g.185144882A>G GRCh38
NC_000004.11:g.186066036A>G , CM000666.1:g.186066036A>G GRCh37
NC_000004.10:g.186303030A>G NCBI36
NG_013001.1:g.6620A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000281456.11:c.230A>G MANE Select ENSP00000281456.5:p.Asn77Ser
ENST00000281456.10:c.230A>G ENSP00000281456.5:p.Asn77Ser
ENST00000491736.1:c.230A>G ENSP00000476711.1:p.Asn77Ser
NM_001151.3:c.230A>G NP_001142.2:p.Asn77Ser
NM_001151.4:c.230A>G MANE Select NP_001142.2:p.Asn77Ser
Search 100 bp 5'
Search 100 bp 3'