Canonical Allele Identifier: CA755935405
Gene:

Linked Data

dbSNP Id: rs1455549393
MyVariant Identifiers: chr2:g.121089913A>C (hg19) chr2:g.120332337A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.120332337A>C , CM000664.2:g.120332337A>C GRCh38
NC_000002.11:g.121089913A>C , CM000664.1:g.121089913A>C GRCh37
NC_000002.10:g.120806383A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011512307.1:c.141+3531A>C XP_011510609.1:n.141+3531A>C
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