Canonical Allele Identifier: CA15701333
Gene: GLYATL2 HGNC NCBI

Linked Data

dbSNP Id: rs496601
gnomAD v2: 11-58631443-A-G
gnomAD v3: 11-58863970-A-G
gnomAD v4: 11-58863970-A-G
MyVariant Identifiers: chr11:g.58631443A>G (hg19) chr11:g.58863970A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.58863970A>G , CM000673.2:g.58863970A>G GRCh38
NC_000011.9:g.58631443A>G , CM000673.1:g.58631443A>G GRCh37
NC_000011.8:g.58388019A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000533636.1:n.61-25602T>C
XM_011544809.3:c.-136-19446T>C XP_011543111.1:n.-136-19446T>C
XM_017017337.2:c.-269-19446T>C XP_016872826.1:n.-269-19446T>C
XM_017017338.2:c.-40-24318T>C XP_016872827.1:n.-40-24318T>C
XM_024448394.1:c.-131-19446T>C XP_024304162.1:n.-131-19446T>C
XM_024448395.1:c.-131-19446T>C XP_024304163.1:n.-131-19446T>C
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