Canonical Allele Identifier: CA2036500865
Gene: KRT6B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52451652T= , CM000674.2:g.52451652T= GRCh38
NC_000012.11:g.52845436T= , CM000674.1:g.52845436T= GRCh37
NC_000012.10:g.51131703T= NCBI36
NG_008299.1:g.5475A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252252.4:c.427A= MANE Select ENSP00000252252.3:p.Ser143=
ENST00000252252.3:c.427A= ENSP00000252252.3:p.Ser143=
NM_005555.3:c.427A= NP_005546.2:p.Ser143=
NM_005555.4:c.427A= MANE Select NP_005546.2:p.Ser143=
Search 100 bp 5'
Search 100 bp 3'