Canonical Allele Identifier: CA1976153187

Gene: GLYATL2

Linked Data

• dbSNP Id: rs496601

Genomic Alleles

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

Transcript Alleles

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