Canonical Allele Identifier: CA237244830
Gene: KRT2 HGNC NCBI

Linked Data

dbSNP Id: rs35544965
MyVariant Identifiers: chr12:g.53045944_53045945insG (hg19) chr12:g.52652160_52652161insG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52652162dup , CM000674.2:g.52652162dup GRCh38
NC_000012.11:g.53045946dup , CM000674.1:g.53045946dup GRCh37
NC_000012.10:g.51332213dup NCBI36
NG_008296.1:g.5015dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000309680.4:c.-19dup MANE Select ENSP00000310861.3:n.-19dup
ENST00000309680.3:c.-19dup ENSP00000310861.3:n.-19dup
NM_000423.2:c.-19dup NP_000414.2:n.-19dup
NM_000423.3:c.-19dup MANE Select NP_000414.2:n.-19dup
Search 100 bp 5'
Search 100 bp 3'