Canonical Allele Identifier: CA2711418015
Gene: MUC22 HGNC NCBI

Linked Data

dbSNP Id: rs2150734296

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31008265A>T , CM000668.2:g.31008265A>T GRCh38
NC_000006.11:g.30976042A>T , CM000668.1:g.30976042A>T GRCh37
NC_000006.10:g.31084021A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001198815.1:c.-38+2132A>T NP_001185744.1:n.-38+2132A>T
NM_001318484.1:c.7+2132A>T NP_001305413.1:n.7+2132A>T