Canonical Allele Identifier: CA2618928481
Gene: KRT6A HGNC NCBI

Linked Data

gnomAD v4: 12-52488563-G-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52488563G>T , CM000674.2:g.52488563G>T GRCh38
NC_000012.11:g.52882347G>T , CM000674.1:g.52882347G>T GRCh37
NC_000012.10:g.51168614G>T NCBI36
NG_008298.1:g.9835C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000330722.7:c.1204-15C>A MANE Select ENSP00000369317.3:n.1204-15C>A
ENST00000330722.6:c.1204-15C>A ENSP00000369317.3:n.1204-15C>A
NM_005554.3:c.1204-15C>A NP_005545.1:n.1204-15C>A
NM_005554.4:c.1204-15C>A MANE Select NP_005545.1:n.1204-15C>A
Search 100 bp 5'
Search 100 bp 3'