Canonical Allele Identifier: CA689834974
Gene: KRT6B HGNC NCBI

Linked Data

dbSNP Id: rs1171602587
gnomAD v3: 12-52447717-C-T
gnomAD v4: 12-52447717-C-T
MyVariant Identifiers: chr12:g.52841501C>T (hg19) chr12:g.52447717C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52447717C>T , CM000674.2:g.52447717C>T GRCh38
NC_000012.11:g.52841501C>T , CM000674.1:g.52841501C>T GRCh37
NC_000012.10:g.51127768C>T NCBI36
NG_008299.1:g.9410G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000252252.4:c.1424+61G>A MANE Select ENSP00000252252.3:n.1424+61G>A
ENST00000252252.3:c.1424+61G>A ENSP00000252252.3:n.1424+61G>A
NM_005555.3:c.1424+61G>A NP_005546.2:n.1424+61G>A
NM_005555.4:c.1424+61G>A MANE Select NP_005546.2:n.1424+61G>A
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