Canonical Allele Identifier: CA2036500347
Gene: KRT6B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52451407C= , CM000674.2:g.52451407C= GRCh38
NC_000012.11:g.52845191C= , CM000674.1:g.52845191C= GRCh37
NC_000012.10:g.51131458C= NCBI36
NG_008299.1:g.5720G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252252.4:c.540+132G= MANE Select ENSP00000252252.3:n.540+132G=
ENST00000252252.3:c.540+132G= ENSP00000252252.3:n.540+132G=
NM_005555.3:c.540+132G= NP_005546.2:n.540+132G=
NM_005555.4:c.540+132G= MANE Select NP_005546.2:n.540+132G=
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