Canonical Allele Identifier: CA384927529
Gene: KRT6B HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.52845463C>A (hg19) chr12:g.52451679C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52451679C>A , CM000674.2:g.52451679C>A GRCh38
NC_000012.11:g.52845463C>A , CM000674.1:g.52845463C>A GRCh37
NC_000012.10:g.51131730C>A NCBI36
NG_008299.1:g.5448G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252252.4:c.400G>T MANE Select ENSP00000252252.3:p.Gly134Cys
ENST00000252252.3:c.400G>T ENSP00000252252.3:p.Gly134Cys
NM_005555.3:c.400G>T NP_005546.2:p.Gly134Cys
NM_005555.4:c.400G>T MANE Select NP_005546.2:p.Gly134Cys
Search 100 bp 5'
Search 100 bp 3'