Canonical Allele Identifier: CA1087405599
Gene: MUC22 HGNC NCBI

Linked Data

dbSNP Id: rs1371917909
gnomAD v3: 6-31008548-C-T
gnomAD v4: 6-31008548-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31008548C>T , CM000668.2:g.31008548C>T GRCh38
NC_000006.11:g.30976325C>T , CM000668.1:g.30976325C>T GRCh37
NC_000006.10:g.31084304C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001198815.1:c.-37-2122C>T NP_001185744.1:n.-37-2122C>T
NM_001318484.1:c.8-2157C>T NP_001305413.1:n.8-2157C>T