Canonical Allele Identifier: CA1618964268
Gene: MUC22 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31008794A= , CM000668.2:g.31008794A= GRCh38
NC_000006.11:g.30976571A= , CM000668.1:g.30976571A= GRCh37
NC_000006.10:g.31084550A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001198815.1:c.-37-1876A= NP_001185744.1:n.-37-1876A=
NM_001318484.1:c.8-1911A= NP_001305413.1:n.8-1911A=