Canonical Allele Identifier: CA566327163

Gene: MUC22

Linked Data

• dbSNP Id: rs1237412503
• gnomAD v2: 6-30976348-C-T
• gnomAD v3: 6-31008571-C-T
• gnomAD v4: 6-31008571-C-T
• MyVariant Identifiers: chr6:g.30976348C>T (hg19) ; chr6:g.31008571C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31008571C>T , CM000668.2:g.31008571C>T	GRCh38
NC_000006.11:g.30976348C>T , CM000668.1:g.30976348C>T	GRCh37
NC_000006.10:g.31084327C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001198815.1:c.-37-2099C>T	NP_001185744.1:n.-37-2099C>T
NM_001318484.1:c.8-2134C>T	NP_001305413.1:n.8-2134C>T