Canonical Allele Identifier: CA2618923500
Gene: KRT75 HGNC NCBI

Linked Data

gnomAD v4: 12-52433786-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52433786G>C , CM000674.2:g.52433786G>C GRCh38
NC_000012.11:g.52827570G>C , CM000674.1:g.52827570G>C GRCh37
NC_000012.10:g.51113837G>C NCBI36
NG_008403.1:g.5541C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000252245.6:c.498+21C>G MANE Select ENSP00000252245.5:n.498+21C>G
ENST00000252245.5:c.498+21C>G ENSP00000252245.5:n.498+21C>G
NM_004693.2:c.498+21C>G NP_004684.2:n.498+21C>G
NM_004693.3:c.498+21C>G MANE Select NP_004684.2:n.498+21C>G
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