Canonical Allele Identifier: CA674857327
Gene:

Linked Data

dbSNP Id: rs1414082593
MyVariant Identifiers: chr11:g.2465770G>A (hg19) chr11:g.2444540G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2444540G>A , CM000673.2:g.2444540G>A GRCh38
NC_000011.9:g.2465770G>A , CM000673.1:g.2465770G>A GRCh37
NC_000011.8:g.2422346G>A NCBI36
NG_008935.1:g.4550G>A , LRG_287:g.4550G>A

Transcript Alleles

HGVS Amino-acid Change
XR_930984.1:n.31C>T
Search 100 bp 5'
Search 100 bp 3'