Canonical Allele Identifier: CA798354212
Gene:

Linked Data

dbSNP Id: rs1469197853
MyVariant Identifiers: chr4:g.75170149T>C (hg19) chr4:g.74304432T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.74304432T>C , CM000666.2:g.74304432T>C GRCh38
NC_000004.11:g.75170149T>C , CM000666.1:g.75170149T>C GRCh37
NC_000004.10:g.75389013T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938877.1:n.120-25654A>G
XR_938877.2:n.126-25654A>G
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