Canonical Allele Identifier: CA2036511395
Gene: KRT75 HGNC NCBI

Linked Data

dbSNP Id: rs1940178671
gnomAD v4: 12-52433740-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52433740A>G , CM000674.2:g.52433740A>G GRCh38
NC_000012.11:g.52827524A>G , CM000674.1:g.52827524A>G GRCh37
NC_000012.10:g.51113791A>G NCBI36
NG_008403.1:g.5587T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000252245.6:c.498+67T>C MANE Select ENSP00000252245.5:n.498+67T>C
ENST00000252245.5:c.498+67T>C ENSP00000252245.5:n.498+67T>C
NM_004693.2:c.498+67T>C NP_004684.2:n.498+67T>C
NM_004693.3:c.498+67T>C MANE Select NP_004684.2:n.498+67T>C
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