Canonical Allele Identifier: CA2575165198
Gene: KRT6A HGNC NCBI

Linked Data

dbSNP Id: rs2120392413

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52488581A>G , CM000674.2:g.52488581A>G GRCh38
NC_000012.11:g.52882365A>G , CM000674.1:g.52882365A>G GRCh37
NC_000012.10:g.51168632A>G NCBI36
NG_008298.1:g.9817T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000330722.7:c.1204-33T>C MANE Select ENSP00000369317.3:n.1204-33T>C
ENST00000330722.6:c.1204-33T>C ENSP00000369317.3:n.1204-33T>C
NM_005554.3:c.1204-33T>C NP_005545.1:n.1204-33T>C
NM_005554.4:c.1204-33T>C MANE Select NP_005545.1:n.1204-33T>C