Canonical Allele Identifier: CA1087405514
Gene: MUC22 HGNC NCBI

Linked Data

dbSNP Id: rs1464006118
gnomAD v3: 6-31008467-G-T
gnomAD v4: 6-31008467-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31008467G>T , CM000668.2:g.31008467G>T GRCh38
NC_000006.11:g.30976244G>T , CM000668.1:g.30976244G>T GRCh37
NC_000006.10:g.31084223G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001198815.1:c.-37-2203G>T NP_001185744.1:n.-37-2203G>T
NM_001318484.1:c.8-2238G>T NP_001305413.1:n.8-2238G>T