Canonical Allele Identifier: CA384981790
Gene: KRT6B HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.52841581G>T (hg19) chr12:g.52447797G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52447797G>T , CM000674.2:g.52447797G>T GRCh38
NC_000012.11:g.52841581G>T , CM000674.1:g.52841581G>T GRCh37
NC_000012.10:g.51127848G>T NCBI36
NG_008299.1:g.9330C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000252252.4:c.1405C>A MANE Select ENSP00000252252.3:p.Leu469Met
ENST00000252252.3:c.1405C>A ENSP00000252252.3:p.Leu469Met
NM_005555.3:c.1405C>A NP_005546.2:p.Leu469Met
NM_005555.4:c.1405C>A MANE Select NP_005546.2:p.Leu469Met
Search 100 bp 5'
Search 100 bp 3'