Canonical Allele Identifier: CA134049513
Gene:

Linked Data

dbSNP Id: rs894556955
MyVariant Identifiers: chr6:g.8525315T>C (hg19) chr6:g.8525082T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.8525082T>C , CM000668.2:g.8525082T>C GRCh38
NC_000006.11:g.8525315T>C , CM000668.1:g.8525315T>C GRCh37
NC_000006.10:g.8470314T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038979.1:n.626-33503T>C
NR_038980.1:n.649-33503T>C
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