Canonical Allele Identifier: CA136813316
Gene: MUC22 HGNC NCBI

Linked Data

dbSNP Id: rs1014771825

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31008499T>C , CM000668.2:g.31008499T>C GRCh38
NC_000006.11:g.30976276T>C , CM000668.1:g.30976276T>C GRCh37
NC_000006.10:g.31084255T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001198815.1:c.-37-2171T>C NP_001185744.1:n.-37-2171T>C
NM_001318484.1:c.8-2206T>C NP_001305413.1:n.8-2206T>C