Canonical Allele Identifier: CA98367559
Gene:

Linked Data

dbSNP Id: rs192648321
gnomAD v2: 4-63423871-C-G
gnomAD v3: 4-62558153-C-G
gnomAD v4: 4-62558153-C-G
MyVariant Identifiers: chr4:g.63423871C>G (hg19) chr4:g.62558153C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62558153C>G , CM000666.2:g.62558153C>G GRCh38
NC_000004.11:g.63423871C>G , CM000666.1:g.63423871C>G GRCh37
NC_000004.10:g.63106466C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938814.1:n.161-5691C>G
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