Canonical Allele Identifier: CA1947457039
Gene: MUC2 HGNC NCBI

Linked Data

dbSNP Id: rs1857868801

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1075609_1075613del , CM000673.2:g.1075609_1075613del GRCh38
NC_000011.9:g.1075609_1075613del , CM000673.1:g.1075609_1075613del GRCh37
NC_000011.8:g.1065609_1065613del NCBI36
NG_051929.1:g.5735_5739del

Transcript Alleles

HGVS Amino-acid Change
ENST00000361558.7:n.104-42_104-38del
ENST00000675028.1:c.77-42_77-38del ENSP00000502432.1:n.77-42_77-38del
NM_002457.3:c.77-42_77-38del NP_002448.3:n.77-42_77-38del
NM_002457.4:c.77-42_77-38del NP_002448.4:n.77-42_77-38del