Canonical Allele Identifier: CA7337114
Community Standard Title: NM_018036.7(ATG2B):c.163-25T>A
Gene: ATG2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.96347366A>T , CM000676.2:g.96347366A>T GRCh38
NC_000014.8:g.96813703A>T , CM000676.1:g.96813703A>T GRCh37
NC_000014.7:g.95883456A>T NCBI36
NG_051091.1:g.21036T>A

Transcript Alleles

HGVS Amino-acid Change
NM_018036.7:c.163-25T>A MANE Select NP_060506.6:n.163-25T>A
ENST00000359933.6:c.163-25T>A MANE Select ENSP00000353010.4:n.163-25T>A
NM_018036.5:c.163-25T>A NP_060506.5:n.163-25T>A
NM_018036.6:c.163-25T>A NP_060506.5:n.163-25T>A
ENST00000359933.5:c.163-25T>A ENSP00000353010.4:n.163-25T>A
XM_006720187.1:c.163-25T>A XP_006720250.1:n.163-25T>A
XM_006720187.2:c.163-25T>A XP_006720250.1:n.163-25T>A
XM_011536888.1:c.163-25T>A XP_011535190.1:n.163-25T>A
XM_017021397.2:c.163-25T>A XP_016876886.1:n.163-25T>A
XR_001750398.1:n.528-25T>A
XR_001750399.1:n.528-25T>A
XR_943482.1:n.528-25T>A
XR_943482.2:n.528-25T>A
XR_943483.1:n.528-25T>A