Canonical Allele Identifier: CA472358101
Gene: MUC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.1075663G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1075663G>T , CM000673.2:g.1075663G>T GRCh38
NC_000011.9:g.1075663G>T , CM000673.1:g.1075663G>T GRCh37
NC_000011.8:g.1065663G>T NCBI36
NG_051929.1:g.5789G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000361558.7:n.116G>T
ENST00000675028.1:c.89G>T ENSP00000502432.1:p.Arg30Leu
NM_002457.3:c.89G>T NP_002448.3:p.Arg30Leu
NM_002457.4:c.89G>T NP_002448.4:p.Arg30Leu
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