Canonical Allele Identifier: CA2712340547
Gene: CCDC162P HGNC NCBI

Linked Data

dbSNP Id: rs1741930

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.109198594T>C , CM000668.2:g.109198594T>C GRCh38
NC_000006.11:g.109519797T>C , CM000668.1:g.109519797T>C GRCh37
NC_000006.10:g.109626490T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000368966.10:n.784+82T>C
ENST00000640755.1:n.867+82T>C
ENST00000640771.1:n.865+82T>C
ENST00000417143.3:c.784+82T>C ENSP00000475092.1:n.784+82T>C
XR_942852.1:n.809+82T>C
NR_152435.1:n.867+82T>C