Canonical Allele Identifier: CA671342850
Gene: MUC2 HGNC NCBI

Linked Data

dbSNP Id: rs1478513168

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1075527_1075532del , CM000673.2:g.1075527_1075532del GRCh38
NC_000011.9:g.1075527_1075532del , CM000673.1:g.1075527_1075532del GRCh37
NC_000011.8:g.1065527_1065532del NCBI36
NG_051929.1:g.5653_5658del

Transcript Alleles

HGVS Amino-acid Change
ENST00000361558.7:n.104-124_104-119del
ENST00000675028.1:c.77-124_77-119del ENSP00000502432.1:n.77-124_77-119del
NM_002457.3:c.77-124_77-119del NP_002448.3:n.77-124_77-119del
NM_002457.4:c.77-124_77-119del NP_002448.4:n.77-124_77-119del