Canonical Allele Identifier: CA759294229
Gene:

Linked Data

dbSNP Id: rs1369634036
MyVariant Identifiers: chr2:g.156726692C>A (hg19) chr2:g.155870180C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.155870180C>A , CM000664.2:g.155870180C>A GRCh38
NC_000002.11:g.156726692C>A , CM000664.1:g.156726692C>A GRCh37
NC_000002.10:g.156434938C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923501.1:n.320-2993G>T
XR_001739749.1:n.331-29196G>T
XR_001739750.1:n.331-29196G>T
XR_001739751.1:n.331-29196G>T
XR_923501.2:n.331-2993G>T
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