Canonical Allele Identifier: CA1618986584
Gene: HCG22 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31057031A= , CM000668.2:g.31057031A= GRCh38
NC_000006.11:g.31024808A= , CM000668.1:g.31024808A= GRCh37
NC_000006.10:g.31132787A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_003948.2:n.1700+121A=
NR_003948.3:n.1701+121A=
NR_145427.1:n.1192+121A=
NR_145427.2:n.1193+121A=
ENST00000426185.1:n.1511+121A=
ENST00000565192.1:n.1192+121A=
ENST00000566475.1:n.300-2377A=
ENST00000646461.3:c.876+121A= ENSP00000507162.2:n.876+121A=