Canonical Allele Identifier: CA384973535
Gene: KRT75 HGNC NCBI

Linked Data

gnomAD v4: 12-52433842-T-A
MyVariant Identifiers: chr12:g.52827626T>A (hg19) chr12:g.52433842T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52433842T>A , CM000674.2:g.52433842T>A GRCh38
NC_000012.11:g.52827626T>A , CM000674.1:g.52827626T>A GRCh37
NC_000012.10:g.51113893T>A NCBI36
NG_008403.1:g.5485A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252245.6:c.463A>T MANE Select ENSP00000252245.5:p.Thr155Ser
ENST00000252245.5:c.463A>T ENSP00000252245.5:p.Thr155Ser
NM_004693.2:c.463A>T NP_004684.2:p.Thr155Ser
NM_004693.3:c.463A>T MANE Select NP_004684.2:p.Thr155Ser
Search 100 bp 5'
Search 100 bp 3'