Canonical Allele Identifier: CA2618924890
Gene: KRT6B HGNC NCBI

Linked Data

gnomAD v4: 12-52451418-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52451418C>A , CM000674.2:g.52451418C>A GRCh38
NC_000012.11:g.52845202C>A , CM000674.1:g.52845202C>A GRCh37
NC_000012.10:g.51131469C>A NCBI36
NG_008299.1:g.5709G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252252.4:c.540+121G>T MANE Select ENSP00000252252.3:n.540+121G>T
ENST00000252252.3:c.540+121G>T ENSP00000252252.3:n.540+121G>T
NM_005555.3:c.540+121G>T NP_005546.2:n.540+121G>T
NM_005555.4:c.540+121G>T MANE Select NP_005546.2:n.540+121G>T
Search 100 bp 5'
Search 100 bp 3'