Canonical Allele Identifier: CA1955524061
Gene: SAA1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.18269975A= , CM000673.2:g.18269975A= GRCh38
NC_000011.9:g.18291522A= , CM000673.1:g.18291522A= GRCh37
NC_000011.8:g.18248098A= NCBI36
NG_021330.1:g.8715A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000405158.2:c.*120A= ENSP00000384906.2:n.*120A=
NM_000331.4:c.*120A= NP_000322.2:n.*120A=
NM_001178006.1:c.*120A= NP_001171477.1:n.*120A=
NM_199161.3:c.*120A= NP_954630.1:n.*120A=
NM_000331.5:c.*120A= NP_000322.2:n.*120A=
NM_001178006.2:c.*120A= NP_001171477.1:n.*120A=
NM_199161.4:c.*120A= NP_954630.1:n.*120A=
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