Canonical Allele Identifier: CA821223468
Gene:

Linked Data

dbSNP Id: rs1313660703
MyVariant Identifiers: chr6:g.156133429G>T (hg19) chr6:g.155812295G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155812295G>T , CM000668.2:g.155812295G>T GRCh38
NC_000006.11:g.156133429G>T , CM000668.1:g.156133429G>T GRCh37
NC_000006.10:g.156175121G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943142.1:n.79+18876G>T
XR_943146.1:n.645-256C>A
XR_001744423.1:n.699-256C>A
XR_001744424.1:n.79+18876G>T
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