Canonical Allele Identifier: CA1097636410
Gene: AMZ1 HGNC NCBI

Linked Data

dbSNP Id: rs1789513363
gnomAD v3: 7-2723771-T-C
gnomAD v4: 7-2723771-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.2723771T>C , CM000669.2:g.2723771T>C GRCh38
NC_000007.13:g.2763405T>C , CM000669.1:g.2763405T>C GRCh37
NC_000007.12:g.2729931T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000489665.1:n.550+13955T>C
XM_011515151.1:c.778+13955T>C XP_011513453.1:n.778+13955T>C
NM_001321766.1:c.948+13955T>C NP_001308695.1:n.948+13955T>C
XM_011515151.3:c.778+13955T>C XP_011513453.1:n.778+13955T>C
XM_017011774.2:c.778+13955T>C XP_016867263.1:n.778+13955T>C
NM_001321766.2:c.948+13955T>C NP_001308695.1:n.948+13955T>C
NM_001384740.1:c.948+13955T>C NP_001371669.1:n.948+13955T>C
NM_001384741.1:c.779-7250T>C NP_001371670.1:n.779-7250T>C
NM_001384742.1:c.779-710T>C NP_001371671.1:n.779-710T>C