Canonical Allele Identifier: CA837193631
Gene: AMZ1 HGNC NCBI

Linked Data

dbSNP Id: rs1325634211
gnomAD v3: 7-2723768-G-A
gnomAD v4: 7-2723768-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.2723768G>A , CM000669.2:g.2723768G>A GRCh38
NC_000007.13:g.2763402G>A , CM000669.1:g.2763402G>A GRCh37
NC_000007.12:g.2729928G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000489665.1:n.550+13952G>A
XM_011515151.1:c.778+13952G>A XP_011513453.1:n.778+13952G>A
NM_001321766.1:c.948+13952G>A NP_001308695.1:n.948+13952G>A
XM_011515151.3:c.778+13952G>A XP_011513453.1:n.778+13952G>A
XM_017011774.2:c.778+13952G>A XP_016867263.1:n.778+13952G>A
NM_001321766.2:c.948+13952G>A NP_001308695.1:n.948+13952G>A
NM_001384740.1:c.948+13952G>A NP_001371669.1:n.948+13952G>A
NM_001384741.1:c.779-7253G>A NP_001371670.1:n.779-7253G>A
NM_001384742.1:c.779-713G>A NP_001371671.1:n.779-713G>A