Canonical Allele Identifier: CA820839136
Gene:

Linked Data

dbSNP Id: rs1383143696
MyVariant Identifiers: chr6:g.151954567T>C (hg19) chr6:g.151633432T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151633432T>C , CM000668.2:g.151633432T>C GRCh38
NC_000006.11:g.151954567T>C , CM000668.1:g.151954567T>C GRCh37
NC_000006.10:g.151996260T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943115.1:n.2496+3450T>C
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