Canonical Allele Identifier: CA1947456990
Gene: MUC2 HGNC NCBI

Linked Data

dbSNP Id: rs1857867731
gnomAD v4: 11-1075568-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1075568T>C , CM000673.2:g.1075568T>C GRCh38
NC_000011.9:g.1075568T>C , CM000673.1:g.1075568T>C GRCh37
NC_000011.8:g.1065568T>C NCBI36
NG_051929.1:g.5694T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000361558.7:n.104-83T>C
ENST00000675028.1:c.77-83T>C ENSP00000502432.1:n.77-83T>C
NM_002457.3:c.77-83T>C NP_002448.3:n.77-83T>C
NM_002457.4:c.77-83T>C NP_002448.4:n.77-83T>C