Canonical Allele Identifier: CA59107069
Gene:

Linked Data

dbSNP Id: rs770198573
MyVariant Identifiers: chr2:g.156726952C>T (hg19) chr2:g.155870440C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.155870440C>T , CM000664.2:g.155870440C>T GRCh38
NC_000002.11:g.156726952C>T , CM000664.1:g.156726952C>T GRCh37
NC_000002.10:g.156435198C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923501.1:n.320-3253G>A
XR_001739749.1:n.331-29456G>A
XR_001739750.1:n.331-29456G>A
XR_001739751.1:n.331-29456G>A
XR_923501.2:n.331-3253G>A
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