Canonical Allele Identifier: CA821226234
Gene:

Linked Data

dbSNP Id: rs1315309693
MyVariant Identifiers: chr6:g.156138802T>C (hg19) chr6:g.155817668T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155817668T>C , CM000668.2:g.155817668T>C GRCh38
NC_000006.11:g.156138802T>C , CM000668.1:g.156138802T>C GRCh37
NC_000006.10:g.156180494T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943142.1:n.79+24249T>C
XR_943146.1:n.552-2998A>G
XR_001744423.1:n.606-2998A>G
XR_001744424.1:n.79+24249T>C
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