Canonical Allele Identifier: CA136813381
Gene: MUC22 HGNC NCBI

Linked Data

dbSNP Id: rs886531342
gnomAD v3: 6-31008762-G-T
gnomAD v4: 6-31008762-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31008762G>T , CM000668.2:g.31008762G>T GRCh38
NC_000006.11:g.30976539G>T , CM000668.1:g.30976539G>T GRCh37
NC_000006.10:g.31084518G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001198815.1:c.-37-1908G>T NP_001185744.1:n.-37-1908G>T
NM_001318484.1:c.8-1943G>T NP_001305413.1:n.8-1943G>T