Canonical Allele Identifier: CA136813408
Gene: MUC22 HGNC NCBI

Linked Data

dbSNP Id: rs1027596602
gnomAD v3: 6-31008894-T-C
gnomAD v4: 6-31008894-T-C
MyVariant Identifiers: chr6:g.30976671T>C (hg19) chr6:g.31008894T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31008894T>C , CM000668.2:g.31008894T>C GRCh38
NC_000006.11:g.30976671T>C , CM000668.1:g.30976671T>C GRCh37
NC_000006.10:g.31084650T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001198815.1:c.-37-1776T>C NP_001185744.1:n.-37-1776T>C
NM_001318484.1:c.8-1811T>C NP_001305413.1:n.8-1811T>C
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