Canonical Allele Identifier: CA797158622
Gene:

Linked Data

dbSNP Id: rs1486901873
gnomAD v3: 4-62558135-T-C
gnomAD v4: 4-62558135-T-C
MyVariant Identifiers: chr4:g.63423853T>C (hg19) chr4:g.62558135T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62558135T>C , CM000666.2:g.62558135T>C GRCh38
NC_000004.11:g.63423853T>C , CM000666.1:g.63423853T>C GRCh37
NC_000004.10:g.63106448T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938814.1:n.161-5709T>C
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