Canonical Allele Identifier: CA821226209
Gene:

Linked Data

dbSNP Id: rs1385767275
gnomAD v3: 6-155817564-C-G
gnomAD v4: 6-155817564-C-G
MyVariant Identifiers: chr6:g.156138698C>G (hg19) chr6:g.155817564C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155817564C>G , CM000668.2:g.155817564C>G GRCh38
NC_000006.11:g.156138698C>G , CM000668.1:g.156138698C>G GRCh37
NC_000006.10:g.156180390C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943142.1:n.79+24145C>G
XR_943146.1:n.552-2894G>C
XR_001744423.1:n.606-2894G>C
XR_001744424.1:n.79+24145C>G
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