Canonical Allele Identifier: CA1619049684
Gene: HCG27 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31202751A= , CM000668.2:g.31202751A= GRCh38
NC_000006.11:g.31170528A= , CM000668.1:g.31170528A= GRCh37
NC_000006.10:g.31278507A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_026791.1:n.503A=
ENST00000383331.4:c.503A=
ENST00000415276.1:n.421A=
ENST00000424675.1:c.424A=