Canonical Allele Identifier: CA1618964304
Gene: MUC22 HGNC NCBI

Linked Data

dbSNP Id: rs1763691612

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31008904T>A , CM000668.2:g.31008904T>A GRCh38
NC_000006.11:g.30976681T>A , CM000668.1:g.30976681T>A GRCh37
NC_000006.10:g.31084660T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001198815.1:c.-37-1766T>A NP_001185744.1:n.-37-1766T>A
NM_001318484.1:c.8-1801T>A NP_001305413.1:n.8-1801T>A