Canonical Allele Identifier: CA472359313
Gene: MUC2 HGNC NCBI

Linked Data

dbSNP Id: rs564228906
gnomAD v2: 11-1075789-A-T
gnomAD v4: 11-1075789-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1075789A>T , CM000673.2:g.1075789A>T GRCh38
NC_000011.9:g.1075789A>T , CM000673.1:g.1075789A>T GRCh37
NC_000011.8:g.1065789A>T NCBI36
NG_051929.1:g.5915A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000361558.7:n.242A>T
ENST00000675028.1:c.215A>T ENSP00000502432.1:p.Lys72Met
NM_002457.3:c.215A>T NP_002448.3:p.Lys72Met
NM_002457.4:c.215A>T NP_002448.4:p.Lys72Met