Canonical Allele Identifier: CA2611850534
Gene: MUC2 HGNC NCBI

Linked Data

gnomAD v4: 11-1100043-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1100043G>T , CM000673.2:g.1100043G>T GRCh38
NC_000011.9:g.1093951G>T , CM000673.1:g.1093951G>T GRCh37
NC_000011.8:g.1083951G>T NCBI36
NG_051929.1:g.32070G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000361558.7:n.9809+18G>T
ENST00000674892.1:c.256+18G>T ENSP00000501871.1:n.256+18G>T