Canonical Allele Identifier: CA830286056
Gene:

Linked Data

dbSNP Id: rs1474125777
MyVariant Identifiers: chr6:g.98462611T>C (hg19) chr6:g.98014735T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98014735T>C , CM000668.2:g.98014735T>C GRCh38
NC_000006.11:g.98462611T>C , CM000668.1:g.98462611T>C GRCh37
NC_000006.10:g.98569332T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_245563.2:n.371+45269T>C
XR_942809.1:n.371+45269T>C
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