Canonical Allele Identifier: CA1519346943
Gene: SLC25A4 HGNC NCBI

Linked Data

dbSNP Id: rs1579209351

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.185144746C>T , CM000666.2:g.185144746C>T GRCh38
NC_000004.11:g.186065900C>T , CM000666.1:g.186065900C>T GRCh37
NC_000004.10:g.186302894C>T NCBI36
NG_013001.1:g.6484C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000281456.11:c.112-18C>T MANE Select ENSP00000281456.5:n.112-18C>T
ENST00000281456.10:c.112-18C>T ENSP00000281456.5:n.112-18C>T
ENST00000491736.1:c.112-18C>T ENSP00000476711.1:n.112-18C>T
NM_001151.3:c.112-18C>T NP_001142.2:n.112-18C>T
NM_001151.4:c.112-18C>T MANE Select NP_001142.2:n.112-18C>T