Canonical Allele Identifier: CA55082075
Gene:

Linked Data

dbSNP Id: rs1025144058
MyVariant Identifiers: chr2:g.123641736T>G (hg19) chr2:g.122884160T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122884160T>G , CM000664.2:g.122884160T>G GRCh38
NC_000002.11:g.123641736T>G , CM000664.1:g.123641736T>G GRCh37
NC_000002.10:g.123358206T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923292.1:n.1125-782T>G
XR_001739692.1:n.1451-782T>G
XR_923292.2:n.1358-782T>G
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