Canonical Allele Identifier: CA479848112
Gene: KRT6B HGNC NCBI

Linked Data

gnomAD v4: 12-52451557-A-G
MyVariant Identifiers: chr12:g.52845341A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52451557A>G , CM000674.2:g.52451557A>G GRCh38
NC_000012.11:g.52845341A>G , CM000674.1:g.52845341A>G GRCh37
NC_000012.10:g.51131608A>G NCBI36
NG_008299.1:g.5570T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000252252.4:c.522T>C MANE Select ENSP00000252252.3:p.Phe174=
ENST00000252252.3:c.522T>C ENSP00000252252.3:p.Phe174=
NM_005555.3:c.522T>C NP_005546.2:p.Phe174=
NM_005555.4:c.522T>C MANE Select NP_005546.2:p.Phe174=
Search 100 bp 5'
Search 100 bp 3'