Canonical Allele Identifier: CA384927054
Gene: KRT6B HGNC NCBI

Linked Data

gnomAD v4: 12-52451576-T-C
MyVariant Identifiers: chr12:g.52845360T>C (hg19) chr12:g.52451576T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52451576T>C , CM000674.2:g.52451576T>C GRCh38
NC_000012.11:g.52845360T>C , CM000674.1:g.52845360T>C GRCh37
NC_000012.10:g.51131627T>C NCBI36
NG_008299.1:g.5551A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000252252.4:c.503A>G MANE Select ENSP00000252252.3:p.Lys168Arg
ENST00000252252.3:c.503A>G ENSP00000252252.3:p.Lys168Arg
NM_005555.3:c.503A>G NP_005546.2:p.Lys168Arg
NM_005555.4:c.503A>G MANE Select NP_005546.2:p.Lys168Arg
Search 100 bp 5'
Search 100 bp 3'