Canonical Allele Identifier: CA134049512
Gene:

Linked Data

dbSNP Id: rs1055843413
MyVariant Identifiers: chr6:g.8525314T>G (hg19) chr6:g.8525081T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.8525081T>G , CM000668.2:g.8525081T>G GRCh38
NC_000006.11:g.8525314T>G , CM000668.1:g.8525314T>G GRCh37
NC_000006.10:g.8470313T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038979.1:n.626-33504T>G
NR_038980.1:n.649-33504T>G
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