Canonical Allele Identifier: CA472359195
Gene: MUC2 HGNC NCBI

Linked Data

dbSNP Id: rs752816609
MyVariant Identifiers: chr11:g.1075777G>T (hg19) chr11:g.1075777G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1075777G>T , CM000673.2:g.1075777G>T GRCh38
NC_000011.9:g.1075777G>T , CM000673.1:g.1075777G>T GRCh37
NC_000011.8:g.1065777G>T NCBI36
NG_051929.1:g.5903G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000361558.7:n.230G>T
ENST00000675028.1:c.203G>T ENSP00000502432.1:p.Arg68Leu
NM_002457.3:c.203G>T NP_002448.3:p.Arg68Leu
NM_002457.4:c.203G>T NP_002448.4:p.Arg68Leu
Search 100 bp 5'
Search 100 bp 3'