Canonical Allele Identifier: CA566327160

Gene: MUC22

Linked Data

• dbSNP Id: rs1344710221
• gnomAD v2: 6-30976344-G-T
• gnomAD v3: 6-31008567-G-T
• gnomAD v4: 6-31008567-G-T
• COSMIC: COSN23962795
• MyVariant Identifiers: chr6:g.30976344G>T (hg19) ; chr6:g.31008567G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31008567G>T , CM000668.2:g.31008567G>T	GRCh38
NC_000006.11:g.30976344G>T , CM000668.1:g.30976344G>T	GRCh37
NC_000006.10:g.31084323G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001198815.1:c.-37-2103G>T	NP_001185744.1:n.-37-2103G>T
NM_001318484.1:c.8-2138G>T	NP_001305413.1:n.8-2138G>T