Canonical Allele Identifier: CA362935170
Gene: NKAPL HGNC NCBI

Linked Data

dbSNP Id: rs1635
MyVariant Identifiers: chr6:g.28227604C>G (hg19) chr6:g.28259826C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.28259826C>G , CM000668.2:g.28259826C>G GRCh38
NC_000006.11:g.28227604C>G , CM000668.1:g.28227604C>G GRCh37
NC_000006.10:g.28335583C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000343684.4:c.455C>G MANE Select ENSP00000345716.3:p.Thr152Ser
ENST00000343684.3:c.455C>G ENSP00000345716.3:p.Thr152Ser
NM_001007531.2:c.455C>G NP_001007532.1:p.Thr152Ser
NM_001007531.3:c.455C>G MANE Select NP_001007532.1:p.Thr152Ser
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