Canonical Allele Identifier: CA566327165

Gene: MUC22

Linked Data

• dbSNP Id: rs1425104831
• gnomAD v2: 6-30976368-C-T
• gnomAD v3: 6-31008591-C-T
• gnomAD v4: 6-31008591-C-T
• MyVariant Identifiers: chr6:g.30976368C>T (hg19) ; chr6:g.31008591C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31008591C>T , CM000668.2:g.31008591C>T	GRCh38
NC_000006.11:g.30976368C>T , CM000668.1:g.30976368C>T	GRCh37
NC_000006.10:g.31084347C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001198815.1:c.-37-2079C>T	NP_001185744.1:n.-37-2079C>T
NM_001318484.1:c.8-2114C>T	NP_001305413.1:n.8-2114C>T