Canonical Allele Identifier: CA54965531
Gene:

Linked Data

dbSNP Id: rs975383015
MyVariant Identifiers: chr2:g.123126922A>T (hg19) chr2:g.122369346A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122369346A>T , CM000664.2:g.122369346A>T GRCh38
NC_000002.11:g.123126922A>T , CM000664.1:g.123126922A>T GRCh37
NC_000002.10:g.122843392A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923278.1:n.556-23617A>T
XR_001739684.1:n.556-23617A>T
Search 100 bp 5'
Search 100 bp 3'