Canonical Allele Identifier: CA472358141
Gene: MUC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.1075666A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1075666A>T , CM000673.2:g.1075666A>T GRCh38
NC_000011.9:g.1075666A>T , CM000673.1:g.1075666A>T GRCh37
NC_000011.8:g.1065666A>T NCBI36
NG_051929.1:g.5792A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000361558.7:n.119A>T
ENST00000675028.1:c.92A>T ENSP00000502432.1:p.Asn31Ile
NM_002457.3:c.92A>T NP_002448.3:p.Asn31Ile
NM_002457.4:c.92A>T NP_002448.4:p.Asn31Ile