Canonical Allele Identifier: CA59107063
Gene:

Linked Data

dbSNP Id: rs939961433
MyVariant Identifiers: chr2:g.156726899C>T (hg19) chr2:g.155870387C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.155870387C>T , CM000664.2:g.155870387C>T GRCh38
NC_000002.11:g.156726899C>T , CM000664.1:g.156726899C>T GRCh37
NC_000002.10:g.156435145C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923501.1:n.320-3200G>A
XR_001739749.1:n.331-29403G>A
XR_001739750.1:n.331-29403G>A
XR_001739751.1:n.331-29403G>A
XR_923501.2:n.331-3200G>A
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