Canonical Allele Identifier: CA2618924496
Gene: KRT6B HGNC NCBI

Linked Data

gnomAD v4: 12-52447634-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52447634G>A , CM000674.2:g.52447634G>A GRCh38
NC_000012.11:g.52841418G>A , CM000674.1:g.52841418G>A GRCh37
NC_000012.10:g.51127685G>A NCBI36
NG_008299.1:g.9493C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000252252.4:c.1425-61C>T MANE Select ENSP00000252252.3:n.1425-61C>T
ENST00000252252.3:c.1425-61C>T ENSP00000252252.3:n.1425-61C>T
NM_005555.3:c.1425-61C>T NP_005546.2:n.1425-61C>T
NM_005555.4:c.1425-61C>T MANE Select NP_005546.2:n.1425-61C>T
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