Canonical Allele Identifier: CA756174460
Gene:

Linked Data

dbSNP Id: rs1230377285
MyVariant Identifiers: chr2:g.123126684T>C (hg19) chr2:g.122369108T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122369108T>C , CM000664.2:g.122369108T>C GRCh38
NC_000002.11:g.123126684T>C , CM000664.1:g.123126684T>C GRCh37
NC_000002.10:g.122843154T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923278.1:n.556-23855T>C
XR_001739684.1:n.556-23855T>C
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