Canonical Allele Identifier: CA862568244
Gene:

Linked Data

dbSNP Id: rs534965290
gnomAD v3: 9-25551487-T-G
gnomAD v4: 9-25551487-T-G
MyVariant Identifiers: chr9:g.25551485T>G (hg19) chr9:g.25551487T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.25551487T>G , CM000671.2:g.25551487T>G GRCh38
NC_000009.11:g.25551485T>G , CM000671.1:g.25551485T>G GRCh37
NC_000009.10:g.25541485T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_929525.1:n.50-915A>C
XR_929525.2:n.674-915A>C
Search 100 bp 5'
Search 100 bp 3'