Canonical Allele Identifier: CA2618924511
Gene: KRT6B HGNC NCBI

Linked Data

gnomAD v4: 12-52447667-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52447667T>G , CM000674.2:g.52447667T>G GRCh38
NC_000012.11:g.52841451T>G , CM000674.1:g.52841451T>G GRCh37
NC_000012.10:g.51127718T>G NCBI36
NG_008299.1:g.9460A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000252252.4:c.1425-94A>C MANE Select ENSP00000252252.3:n.1425-94A>C
ENST00000252252.3:c.1425-94A>C ENSP00000252252.3:n.1425-94A>C
NM_005555.3:c.1425-94A>C NP_005546.2:n.1425-94A>C
NM_005555.4:c.1425-94A>C MANE Select NP_005546.2:n.1425-94A>C
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