Canonical Allele Identifier: CA687013203
Gene:

Linked Data

dbSNP Id: rs1259294122
MyVariant Identifiers: chr12:g.28198162G>C (hg19) chr12:g.28045229G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.28045229G>C , CM000674.2:g.28045229G>C GRCh38
NC_000012.11:g.28198162G>C , CM000674.1:g.28198162G>C GRCh37
NC_000012.10:g.28089429G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_931460.1:n.154-6271C>G
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