Canonical Allele Identifier: CA2677946793
Gene: HCG27 HGNC NCBI

Linked Data

gnomAD v4: 6-31200085-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31200085G>T , CM000668.2:g.31200085G>T GRCh38
NC_000006.11:g.31167862G>T , CM000668.1:g.31167862G>T GRCh37
NC_000006.10:g.31275841G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000383331.4:c.123+2203G>T
ENST00000414008.2:n.192G>T
ENST00000424675.1:c.44+1904G>T
NR_026791.1:n.123+2203G>T