Canonical Allele Identifier: CA16594374
Gene: BACE2 HGNC NCBI

Linked Data

dbSNP Id: rs6517656

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.41211811G>A , CM000683.2:g.41211811G>A GRCh38
NC_000021.8:g.42583738G>A , CM000683.1:g.42583738G>A GRCh37
NC_000021.7:g.41505608G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000330333.11:c.313-14455G>A MANE Select ENSP00000332979.6:n.313-14455G>A
ENST00000328735.10:c.313-14455G>A ENSP00000333854.6:n.313-14455G>A
ENST00000330333.10:c.313-14455G>A ENSP00000332979.6:n.313-14455G>A
ENST00000347667.5:c.313-14455G>A ENSP00000327528.4:n.313-14455G>A
NM_012105.4:c.313-14455G>A NP_036237.2:n.313-14455G>A
NM_138991.2:c.313-14455G>A NP_620476.1:n.313-14455G>A
NM_138992.2:c.313-14455G>A NP_620477.1:n.313-14455G>A
XM_017028314.1:c.27+779G>A XP_016883803.1:n.27+779G>A
NM_012105.5:c.313-14455G>A MANE Select NP_036237.2:n.313-14455G>A
NM_138991.3:c.313-14455G>A NP_620476.1:n.313-14455G>A
NM_138992.3:c.313-14455G>A NP_620477.1:n.313-14455G>A