Canonical Allele Identifier: CA678739830
Gene: GLYATL2 HGNC NCBI

Linked Data

dbSNP Id: rs496601

Genomic Alleles

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

Transcript Alleles

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