HGVS | Genome Assembly |
---|---|
NC_000019.10:g.38930455_38930476del , CM000681.2:g.38930455_38930476del | GRCh38 |
NC_000019.9:g.39421095_39421116del , CM000681.1:g.39421095_39421116del | GRCh37 |
NC_000019.8:g.44112935_44112956del | NCBI36 |
NG_029222.1:g.4748_4769del | |
NG_031865.1:g.5422_5443del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000221431.11:c.262_267+16del | ||
ENST00000221431.10:c.262_267+16del | ||
ENST00000430193.7:c.262_267+16del | ||
ENST00000455102.6:c.262_267+16del | ||
ENST00000593754.1:c.262_267+16del | ||
ENST00000598343.5:c.262_267+16del | ||
ENST00000598598.5:n.289_294+16del | ||
ENST00000599996.1:c.476-4175_476-4154del | ||
ENST00000600042.5:c.262_267+16del | ||
NM_001145901.1:c.262_267+16del | ||
NM_017827.3:c.262_267+16del | ||
NM_001145901.2:c.262_267+16del | ||
NM_017827.4:c.262_267+16del |