Canonical Allele Identifier: CA756174479
Gene:

Linked Data

dbSNP Id: rs900657160
MyVariant Identifiers: chr2:g.123126718G>A (hg19) chr2:g.122369142G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122369142G>A , CM000664.2:g.122369142G>A GRCh38
NC_000002.11:g.123126718G>A , CM000664.1:g.123126718G>A GRCh37
NC_000002.10:g.122843188G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923278.1:n.556-23821G>A
XR_001739684.1:n.556-23821G>A
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