HGVS | Genome Assembly |
---|---|
NC_000003.12:g.98585705C= , CM000665.2:g.98585705C= | GRCh38 |
NC_000003.11:g.98304549C= , CM000665.1:g.98304549C= | GRCh37 |
NC_000003.10:g.99787239C= | NCBI36 |
NG_015994.1:g.12907G= | |
NG_015994.2:g.12907G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000647941.2:c.954-46G= MANE Select | ENSP00000497326.1:n.954-46G= | |
ENST00000264193.2:c.954-46G= | ENSP00000264193.2:n.954-46G= | |
ENST00000510489.1:n.158G= | ||
NM_000097.5:c.954-46G= | NP_000088.3:n.954-46G= | |
XM_005247125.3:c.954-46G= | XP_005247182.1:n.954-46G= | |
NM_000097.7:c.954-46G= MANE Select | NP_000088.3:n.954-46G= | |
XM_005247125.4:c.954-46G= | XP_005247182.1:n.954-46G= | |
XR_001740025.2:n.1125-46G= | ||
XR_001740026.1:n.1643G= | ||
XR_001740027.1:n.1229-46G= | ||
XR_001740028.1:n.1195-46G= |