Canonical Allele Identifier: CA2036500836
Gene: KRT6B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52451640G= , CM000674.2:g.52451640G= GRCh38
NC_000012.11:g.52845424G= , CM000674.1:g.52845424G= GRCh37
NC_000012.10:g.51131691G= NCBI36
NG_008299.1:g.5487C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252252.4:c.439C= MANE Select ENSP00000252252.3:p.Pro147=
ENST00000252252.3:c.439C= ENSP00000252252.3:p.Pro147=
NM_005555.3:c.439C= NP_005546.2:p.Pro147=
NM_005555.4:c.439C= MANE Select NP_005546.2:p.Pro147=
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