Canonical Allele Identifier: CA2672840920
Gene: SLC25A4 HGNC NCBI

Linked Data

gnomAD v4: 4-185144704-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.185144704T>G , CM000666.2:g.185144704T>G GRCh38
NC_000004.11:g.186065858T>G , CM000666.1:g.186065858T>G GRCh37
NC_000004.10:g.186302852T>G NCBI36
NG_013001.1:g.6442T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000281456.11:c.112-60T>G MANE Select ENSP00000281456.5:n.112-60T>G
ENST00000281456.10:c.112-60T>G ENSP00000281456.5:n.112-60T>G
ENST00000491736.1:c.112-60T>G ENSP00000476711.1:n.112-60T>G
NM_001151.3:c.112-60T>G NP_001142.2:n.112-60T>G
NM_001151.4:c.112-60T>G MANE Select NP_001142.2:n.112-60T>G
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