Canonical Allele Identifier: CA384927607
Gene: KRT6B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52451696G>C , CM000674.2:g.52451696G>C GRCh38
NC_000012.11:g.52845480G>C , CM000674.1:g.52845480G>C GRCh37
NC_000012.10:g.51131747G>C NCBI36
NG_008299.1:g.5431C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000252252.4:c.383C>G MANE Select ENSP00000252252.3:p.Pro128Arg
ENST00000252252.3:c.383C>G ENSP00000252252.3:p.Pro128Arg
NM_005555.3:c.383C>G NP_005546.2:p.Pro128Arg
NM_005555.4:c.383C>G MANE Select NP_005546.2:p.Pro128Arg