Canonical Allele Identifier: CA131177550
Gene:

Linked Data

dbSNP Id: rs948991009
gnomAD v3: 5-162656496-A-G
gnomAD v4: 5-162656496-A-G
MyVariant Identifiers: chr5:g.162083502A>G (hg19) chr5:g.162656496A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.162656496A>G , CM000667.2:g.162656496A>G GRCh38
NC_000005.9:g.162083502A>G , CM000667.1:g.162083502A>G GRCh37
NC_000005.8:g.162016080A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001742958.1:n.418+3606T>C
Search 100 bp 5'
Search 100 bp 3'