Canonical Allele Identifier: CA661147975
Gene: EEF1AKMT2 HGNC NCBI

Linked Data

dbSNP Id: rs1194044964
MyVariant Identifiers: chr10:g.126437937G>C (hg19) chr10:g.124749368G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.124749368G>C , CM000672.2:g.124749368G>C GRCh38
NC_000010.10:g.126437937G>C , CM000672.1:g.126437937G>C GRCh37
NC_000010.9:g.126427927G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000494792.1:c.628+11018C>G
ENST00000495711.2:c.187-882C>G
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