HGVS | Genome Assembly |
---|---|
NC_000003.12:g.49131979A>C , CM000665.2:g.49131979A>C | GRCh38 |
NC_000003.11:g.49169412A>C , CM000665.1:g.49169412A>C | GRCh37 |
NC_000003.10:g.49144416A>C | NCBI36 |
NG_008094.1:g.6188T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000305544.9:c.459+137T>G MANE Select | ENSP00000307156.4:n.459+137T>G | |
ENST00000305544.8:c.459+137T>G | ENSP00000307156.4:n.459+137T>G | |
ENST00000418109.5:c.459+137T>G | ENSP00000388325.1:n.459+137T>G | |
ENST00000494831.1:c.12+137T>G | ENSP00000444751.1:n.12+137T>G | |
NM_002292.3:c.459+137T>G | NP_002283.3:n.459+137T>G | |
XM_005265127.3:c.459+137T>G | XP_005265184.1:n.459+137T>G | |
XM_005265127.4:c.459+137T>G | XP_005265184.1:n.459+137T>G | |
NM_002292.4:c.459+137T>G MANE Select | NP_002283.3:n.459+137T>G |