Canonical Allele Identifier: CA759294279
Gene:

Linked Data

dbSNP Id: rs1183828844
MyVariant Identifiers: chr2:g.156726812T>G (hg19) chr2:g.155870300T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.155870300T>G , CM000664.2:g.155870300T>G GRCh38
NC_000002.11:g.156726812T>G , CM000664.1:g.156726812T>G GRCh37
NC_000002.10:g.156435058T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923501.1:n.320-3113A>C
XR_001739749.1:n.331-29316A>C
XR_001739750.1:n.331-29316A>C
XR_001739751.1:n.331-29316A>C
XR_923501.2:n.331-3113A>C
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