Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.6685984G= , CM000681.2:g.6685984G= | GRCh38 |
| NC_000019.9:g.6685995G= , CM000681.1:g.6685995G= | GRCh37 |
| NC_000019.8:g.6636995G= | NCBI36 |
| NG_009557.1:g.39668C= , LRG_27:g.39668C= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000695651.1:n.2158+140C= | ||
| ENST00000695653.1:c.1719+140C= | ENSP00000512084.1:n.1719+140C= | |
| ENST00000695654.1:c.2835+140C= | ENSP00000512085.1:n.2835+140C= | |
| ENST00000245907.11:c.3810+140C= MANE Select | ENSP00000245907.4:n.3810+140C= | |
| ENST00000245907.10:c.3810+140C= | ENSP00000245907.4:n.3810+140C= | |
| ENST00000596238.1:n.253+140C= | ||
| ENST00000601008.1:c.241+762C= | ENSP00000471384.1:n.241+762C= | |
| NM_000064.3:c.3810+140C= | NP_000055.2:n.3810+140C= | |
| NM_000064.4:c.3810+140C= MANE Select | NP_000055.2:n.3810+140C= |