Canonical Allele Identifier: CA797158465
Gene:

Linked Data

dbSNP Id: rs1272157138
gnomAD v3: 4-62557889-T-A
gnomAD v4: 4-62557889-T-A
MyVariant Identifiers: chr4:g.63423607T>A (hg19) chr4:g.62557889T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62557889T>A , CM000666.2:g.62557889T>A GRCh38
NC_000004.11:g.63423607T>A , CM000666.1:g.63423607T>A GRCh37
NC_000004.10:g.63106202T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938814.1:n.161-5955T>A
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Search 100 bp 3'