Canonical Allele Identifier: CA59107066
Gene:

Linked Data

dbSNP Id: rs900855612
MyVariant Identifiers: chr2:g.156726918A>G (hg19) chr2:g.155870406A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.155870406A>G , CM000664.2:g.155870406A>G GRCh38
NC_000002.11:g.156726918A>G , CM000664.1:g.156726918A>G GRCh37
NC_000002.10:g.156435164A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923501.1:n.320-3219T>C
XR_001739749.1:n.331-29422T>C
XR_001739750.1:n.331-29422T>C
XR_001739751.1:n.331-29422T>C
XR_923501.2:n.331-3219T>C
Search 100 bp 5'
Search 100 bp 3'