Canonical Allele Identifier: CA1947456931
Gene: MUC2 HGNC NCBI

Linked Data

dbSNP Id: rs1857866360
gnomAD v4: 11-1075508-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1075508G>T , CM000673.2:g.1075508G>T GRCh38
NC_000011.9:g.1075508G>T , CM000673.1:g.1075508G>T GRCh37
NC_000011.8:g.1065508G>T NCBI36
NG_051929.1:g.5634G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000361558.7:n.104-143G>T
ENST00000675028.1:c.77-143G>T ENSP00000502432.1:n.77-143G>T
NM_002457.3:c.77-143G>T NP_002448.3:n.77-143G>T
NM_002457.4:c.77-143G>T NP_002448.4:n.77-143G>T