Canonical Allele Identifier: CA449627445
Gene: HCG27 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.31167944T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31200167T>G , CM000668.2:g.31200167T>G GRCh38
NC_000006.11:g.31167944T>G , CM000668.1:g.31167944T>G GRCh37
NC_000006.10:g.31275923T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000383331.4:c.124-2205T>G
ENST00000414008.2:n.274T>G
ENST00000424675.1:c.44+1986T>G
NR_026791.1:n.124-2205T>G