Canonical Allele Identifier: CA1087405755
Gene: MUC22 HGNC NCBI

Linked Data

dbSNP Id: rs1763662959
gnomAD v3: 6-31008585-G-T
gnomAD v4: 6-31008585-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31008585G>T , CM000668.2:g.31008585G>T GRCh38
NC_000006.11:g.30976362G>T , CM000668.1:g.30976362G>T GRCh37
NC_000006.10:g.31084341G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001198815.1:c.-37-2085G>T NP_001185744.1:n.-37-2085G>T
NM_001318484.1:c.8-2120G>T NP_001305413.1:n.8-2120G>T