Canonical Allele Identifier: CA2618924500
Gene: KRT6B HGNC NCBI

Linked Data

gnomAD v4: 12-52447648-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52447648A>G , CM000674.2:g.52447648A>G GRCh38
NC_000012.11:g.52841432A>G , CM000674.1:g.52841432A>G GRCh37
NC_000012.10:g.51127699A>G NCBI36
NG_008299.1:g.9479T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000252252.4:c.1425-75T>C MANE Select ENSP00000252252.3:n.1425-75T>C
ENST00000252252.3:c.1425-75T>C ENSP00000252252.3:n.1425-75T>C
NM_005555.3:c.1425-75T>C NP_005546.2:n.1425-75T>C
NM_005555.4:c.1425-75T>C MANE Select NP_005546.2:n.1425-75T>C
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