Canonical Allele Identifier: CA823869721

Gene: MUC22

Linked Data

• dbSNP Id: rs1272915385
• gnomAD v3: 6-31008530-A-C
• gnomAD v4: 6-31008530-A-C
• MyVariant Identifiers: chr6:g.30976307A>C (hg19) ; chr6:g.31008530A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31008530A>C , CM000668.2:g.31008530A>C	GRCh38
NC_000006.11:g.30976307A>C , CM000668.1:g.30976307A>C	GRCh37
NC_000006.10:g.31084286A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001198815.1:c.-37-2140A>C	NP_001185744.1:n.-37-2140A>C
NM_001318484.1:c.8-2175A>C	NP_001305413.1:n.8-2175A>C