Canonical Allele Identifier: CA2618924501
Gene: KRT6B HGNC NCBI

Linked Data

gnomAD v4: 12-52447650-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52447650G>T , CM000674.2:g.52447650G>T GRCh38
NC_000012.11:g.52841434G>T , CM000674.1:g.52841434G>T GRCh37
NC_000012.10:g.51127701G>T NCBI36
NG_008299.1:g.9477C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000252252.4:c.1425-77C>A MANE Select ENSP00000252252.3:n.1425-77C>A
ENST00000252252.3:c.1425-77C>A ENSP00000252252.3:n.1425-77C>A
NM_005555.3:c.1425-77C>A NP_005546.2:n.1425-77C>A
NM_005555.4:c.1425-77C>A MANE Select NP_005546.2:n.1425-77C>A
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