Canonical Allele Identifier: CA1618964109
Gene: MUC22 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31008470A= , CM000668.2:g.31008470A= GRCh38
NC_000006.11:g.30976247A= , CM000668.1:g.30976247A= GRCh37
NC_000006.10:g.31084226A= NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001198815.1:c.-37-2200A= NP_001185744.1:n.-37-2200A=
NM_001318484.1:c.8-2235A= NP_001305413.1:n.8-2235A=