Canonical Allele Identifier: CA689838467
Gene: KRT6A HGNC NCBI

Linked Data

dbSNP Id: rs1298035420

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52492574T>C , CM000674.2:g.52492574T>C GRCh38
NC_000012.11:g.52886358T>C , CM000674.1:g.52886358T>C GRCh37
NC_000012.10:g.51172625T>C NCBI36
NG_008298.1:g.5824A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000330722.7:c.540+75A>G MANE Select ENSP00000369317.3:n.540+75A>G
ENST00000330722.6:c.540+75A>G ENSP00000369317.3:n.540+75A>G
ENST00000549898.5:n.61+75A>G
NM_005554.3:c.540+75A>G NP_005545.1:n.540+75A>G
NM_005554.4:c.540+75A>G MANE Select NP_005545.1:n.540+75A>G