Canonical Allele Identifier: CA472358916
Gene: MUC2 HGNC NCBI

Linked Data

gnomAD v4: 11-1075746-C-T
MyVariant Identifiers: chr11:g.1075746C>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1075746C>T , CM000673.2:g.1075746C>T GRCh38
NC_000011.9:g.1075746C>T , CM000673.1:g.1075746C>T GRCh37
NC_000011.8:g.1065746C>T NCBI36
NG_051929.1:g.5872C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000361558.7:n.199C>T
ENST00000675028.1:c.172C>T ENSP00000502432.1:p.Pro58Ser
NM_002457.3:c.172C>T NP_002448.3:p.Pro58Ser
NM_002457.4:c.172C>T NP_002448.4:p.Leu58Phe
Search 100 bp 5'
Search 100 bp 3'