Canonical Allele Identifier: CA2036522672
Gene: KRT6A HGNC NCBI

Linked Data

dbSNP Id: rs1226456482

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52492560C>A , CM000674.2:g.52492560C>A GRCh38
NC_000012.11:g.52886344C>A , CM000674.1:g.52886344C>A GRCh37
NC_000012.10:g.51172611C>A NCBI36
NG_008298.1:g.5838G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000330722.7:c.540+89G>T MANE Select ENSP00000369317.3:n.540+89G>T
ENST00000330722.6:c.540+89G>T ENSP00000369317.3:n.540+89G>T
ENST00000549898.5:n.61+89G>T
NM_005554.3:c.540+89G>T NP_005545.1:n.540+89G>T
NM_005554.4:c.540+89G>T MANE Select NP_005545.1:n.540+89G>T