Canonical Allele Identifier: CA8562575
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs759724434
ExAC: 17:39739990 T / C
gnomAD v2: 17-39739990-T-C
gnomAD v3: 17-41583738-T-C
gnomAD v4: 17-41583738-T-C
MyVariant Identifiers: chr17:g.39739990T>C (hg19) chr17:g.41583738T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583738T>C , CM000679.2:g.41583738T>C GRCh38
NC_000017.10:g.39739990T>C , CM000679.1:g.39739990T>C GRCh37
NC_000017.9:g.36993516T>C NCBI36
NG_008624.1:g.8158A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.927+22A>G MANE Select ENSP00000167586.6:n.927+22A>G
ENST00000167586.6:c.927+22A>G ENSP00000167586.6:n.927+22A>G
ENST00000476662.1:n.377+22A>G
NM_000526.4:c.927+22A>G NP_000517.2:n.927+22A>G
NM_000526.5:c.927+22A>G MANE Select NP_000517.3:n.927+22A>G
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