Canonical Allele Identifier: CA837193313
Gene: AMZ1 HGNC NCBI

Linked Data

dbSNP Id: rs1361834284
gnomAD v3: 7-2723382-G-C
gnomAD v4: 7-2723382-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.2723382G>C , CM000669.2:g.2723382G>C GRCh38
NC_000007.13:g.2763016G>C , CM000669.1:g.2763016G>C GRCh37
NC_000007.12:g.2729542G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000489665.1:n.550+13566G>C
XM_011515151.1:c.778+13566G>C XP_011513453.1:n.778+13566G>C
NM_001321766.1:c.948+13566G>C NP_001308695.1:n.948+13566G>C
XM_011515151.3:c.778+13566G>C XP_011513453.1:n.778+13566G>C
XM_017011774.2:c.778+13566G>C XP_016867263.1:n.778+13566G>C
NM_001321766.2:c.948+13566G>C NP_001308695.1:n.948+13566G>C
NM_001384740.1:c.948+13566G>C NP_001371669.1:n.948+13566G>C
NM_001384741.1:c.779-7639G>C NP_001371670.1:n.779-7639G>C
NM_001384742.1:c.779-1099G>C NP_001371671.1:n.779-1099G>C