Canonical Allele Identifier: CA384982123
Gene: KRT6B HGNC NCBI

Linked Data

dbSNP Id: rs1327253901
gnomAD v2: 12-52841641-G-A
gnomAD v3: 12-52447857-G-A
gnomAD v4: 12-52447857-G-A
MyVariant Identifiers: chr12:g.52841641G>A (hg19) chr12:g.52447857G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52447857G>A , CM000674.2:g.52447857G>A GRCh38
NC_000012.11:g.52841641G>A , CM000674.1:g.52841641G>A GRCh37
NC_000012.10:g.51127908G>A NCBI36
NG_008299.1:g.9270C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252252.4:c.1345C>T MANE Select ENSP00000252252.3:p.Gln449Ter
ENST00000252252.3:c.1345C>T ENSP00000252252.3:p.Gln449Ter
NM_005555.3:c.1345C>T NP_005546.2:p.Gln449Ter
NM_005555.4:c.1345C>T MANE Select NP_005546.2:p.Gln449Ter
Search 100 bp 5'
Search 100 bp 3'