Canonical Allele Identifier: CA830286011
Gene:

Linked Data

dbSNP Id: rs1232545078
MyVariant Identifiers: chr6:g.98462452A>G (hg19) chr6:g.98014576A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98014576A>G , CM000668.2:g.98014576A>G GRCh38
NC_000006.11:g.98462452A>G , CM000668.1:g.98462452A>G GRCh37
NC_000006.10:g.98569173A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245563.2:n.371+45110A>G
XR_942809.1:n.371+45110A>G
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