Canonical Allele Identifier: CA797158481
Gene:

Linked Data

dbSNP Id: rs1168055676
gnomAD v3: 4-62557937-T-C
gnomAD v4: 4-62557937-T-C
MyVariant Identifiers: chr4:g.63423655T>C (hg19) chr4:g.62557937T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62557937T>C , CM000666.2:g.62557937T>C GRCh38
NC_000004.11:g.63423655T>C , CM000666.1:g.63423655T>C GRCh37
NC_000004.10:g.63106250T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938814.1:n.161-5907T>C
Search 100 bp 5'
Search 100 bp 3'