Canonical Allele Identifier: CA472358547
Gene: MUC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.1075708A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1075708A>T , CM000673.2:g.1075708A>T GRCh38
NC_000011.9:g.1075708A>T , CM000673.1:g.1075708A>T GRCh37
NC_000011.8:g.1065708A>T NCBI36
NG_051929.1:g.5834A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000361558.7:n.161A>T
ENST00000675028.1:c.134A>T ENSP00000502432.1:p.Tyr45Phe
NM_002457.3:c.134A>T NP_002448.3:p.Tyr45Phe
NM_002457.4:c.134A>T NP_002448.4:p.Tyr45Phe