Canonical Allele Identifier: CA2036493764
Gene: KRT6B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52447695G= , CM000674.2:g.52447695G= GRCh38
NC_000012.11:g.52841479G= , CM000674.1:g.52841479G= GRCh37
NC_000012.10:g.51127746G= NCBI36
NG_008299.1:g.9432C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252252.4:c.1424+83C= MANE Select ENSP00000252252.3:n.1424+83C=
ENST00000252252.3:c.1424+83C= ENSP00000252252.3:n.1424+83C=
NM_005555.3:c.1424+83C= NP_005546.2:n.1424+83C=
NM_005555.4:c.1424+83C= MANE Select NP_005546.2:n.1424+83C=
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