Canonical Allele Identifier: CA384927601
Gene: KRT6B HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.52845478C>T (hg19) chr12:g.52451694C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52451694C>T , CM000674.2:g.52451694C>T GRCh38
NC_000012.11:g.52845478C>T , CM000674.1:g.52845478C>T GRCh37
NC_000012.10:g.51131745C>T NCBI36
NG_008299.1:g.5433G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000252252.4:c.385G>A MANE Select ENSP00000252252.3:p.Val129Met
ENST00000252252.3:c.385G>A ENSP00000252252.3:p.Val129Met
NM_005555.3:c.385G>A NP_005546.2:p.Val129Met
NM_005555.4:c.385G>A MANE Select NP_005546.2:p.Val129Met
Search 100 bp 5'
Search 100 bp 3'