Canonical Allele Identifier: CA298296881
Gene:

Linked Data

dbSNP Id: rs1050174941
gnomAD v3: 18-31756908-T-C
gnomAD v4: 18-31756908-T-C
MyVariant Identifiers: chr18:g.29336871T>C (hg19) chr18:g.31756908T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31756908T>C , CM000680.2:g.31756908T>C GRCh38
NC_000018.9:g.29336871T>C , CM000680.1:g.29336871T>C GRCh37
NC_000018.8:g.27590869T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_935338.1:n.66-5231T>C
Search 100 bp 5'
Search 100 bp 3'