Canonical Allele Identifier: CA817908546
Gene:

Linked Data

dbSNP Id: rs1489910501
MyVariant Identifiers: chr6:g.11943893T>C (hg19) chr6:g.11943660T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.11943660T>C , CM000668.2:g.11943660T>C GRCh38
NC_000006.11:g.11943893T>C , CM000668.1:g.11943893T>C GRCh37
NC_000006.10:g.12051879T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001743976.1:n.348-7875T>C
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