Canonical Allele Identifier: CA823869756
Gene: MUC22 HGNC NCBI

Linked Data

dbSNP Id: rs1027596602
MyVariant Identifiers: chr6:g.30976671T>G (hg19) chr6:g.31008894T>G (hg38)
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Genomic Alleles

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

Transcript Alleles

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