Canonical Allele Identifier: CA136813291
Gene: MUC22 HGNC NCBI

Linked Data

dbSNP Id: rs1053864137
gnomAD v2: 6-30976176-G-A
gnomAD v3: 6-31008399-G-A
gnomAD v4: 6-31008399-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31008399G>A , CM000668.2:g.31008399G>A GRCh38
NC_000006.11:g.30976176G>A , CM000668.1:g.30976176G>A GRCh37
NC_000006.10:g.31084155G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001198815.1:c.-38+2266G>A NP_001185744.1:n.-38+2266G>A
NM_001318484.1:c.7+2266G>A NP_001305413.1:n.7+2266G>A