Canonical Allele Identifier: CA896967434
Gene:

Linked Data

dbSNP Id: rs1366084515
MyVariant Identifiers: chr3:g.109462472G>C (hg19) chr3:g.109743625G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.109743625G>C , CM000665.2:g.109743625G>C GRCh38
NC_000003.11:g.109462472G>C , CM000665.1:g.109462472G>C GRCh37
NC_000003.10:g.110945162G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_924325.1:n.142+63430G>C
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