Canonical Allele Identifier: CA566327151
Gene: MUC22 HGNC NCBI

Linked Data

dbSNP Id: rs778449102
gnomAD v2: 6-30976121-G-T
gnomAD v3: 6-31008344-G-T
gnomAD v4: 6-31008344-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31008344G>T , CM000668.2:g.31008344G>T GRCh38
NC_000006.11:g.30976121G>T , CM000668.1:g.30976121G>T GRCh37
NC_000006.10:g.31084100G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001198815.1:c.-38+2211G>T NP_001185744.1:n.-38+2211G>T
NM_001318484.1:c.7+2211G>T NP_001305413.1:n.7+2211G>T