Canonical Allele Identifier: CA384927462
Gene: KRT6B HGNC NCBI

Linked Data

COSMIC: COSM1322431
MyVariant Identifiers: chr12:g.52845451C>A (hg19) chr12:g.52451667C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52451667C>A , CM000674.2:g.52451667C>A GRCh38
NC_000012.11:g.52845451C>A , CM000674.1:g.52845451C>A GRCh37
NC_000012.10:g.51131718C>A NCBI36
NG_008299.1:g.5460G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252252.4:c.412G>T MANE Select ENSP00000252252.3:p.Val138Phe
ENST00000252252.3:c.412G>T ENSP00000252252.3:p.Val138Phe
NM_005555.3:c.412G>T NP_005546.2:p.Val138Phe
NM_005555.4:c.412G>T MANE Select NP_005546.2:p.Val138Phe
Search 100 bp 5'
Search 100 bp 3'