Canonical Allele Identifier: CA136813270
Gene: MUC22 HGNC NCBI

Linked Data

dbSNP Id: rs545010990
gnomAD v2: 6-30976122-A-T
gnomAD v3: 6-31008345-A-T
gnomAD v4: 6-31008345-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31008345A>T , CM000668.2:g.31008345A>T GRCh38
NC_000006.11:g.30976122A>T , CM000668.1:g.30976122A>T GRCh37
NC_000006.10:g.31084101A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001198815.1:c.-38+2212A>T NP_001185744.1:n.-38+2212A>T
NM_001318484.1:c.7+2212A>T NP_001305413.1:n.7+2212A>T