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Canonical Allele Identifier:
CA467261767
Gene: SLC25A25-AS1
HGNC
NCBI
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh37
chr9:g.130880829G>T
Linked Data - NCBI & NCI
dbSNP:
10987883
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.128118550G>T , CM000671.2:g.128118550G>T
GRCh38
NC_000009.11:g.130880829G>T , CM000671.1:g.130880829G>T
GRCh37
NC_000009.10:g.129920650G>T
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_033374.1:n.185C>A
Search 100 bp 5'
Search 100 bp 3'