Canonical Allele Identifier: CA182706488
Gene: NACA4P HGNC NCBI

Linked Data

dbSNP Id: rs1049912141
MyVariant Identifiers: chr8:g.102375202T>G (hg19) chr8:g.101362974T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.101362974T>G , CM000670.2:g.101362974T>G GRCh38
NC_000008.10:g.102375202T>G , CM000670.1:g.102375202T>G GRCh37
NC_000008.9:g.102444378T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000419462.1:n.285+896T>G
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