Canonical Allele Identifier: CA472358514
Gene: MUC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.1075705A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1075705A>C , CM000673.2:g.1075705A>C GRCh38
NC_000011.9:g.1075705A>C , CM000673.1:g.1075705A>C GRCh37
NC_000011.8:g.1065705A>C NCBI36
NG_051929.1:g.5831A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000361558.7:n.158A>C
ENST00000675028.1:c.131A>C ENSP00000502432.1:p.His44Pro
NM_002457.3:c.131A>C NP_002448.3:p.His44Pro
NM_002457.4:c.131A>C NP_002448.4:p.His44Pro