Canonical Allele Identifier: CA449639799
Gene: HCG27 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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