HGVS | Genome Assembly |
---|---|
NC_000013.11:g.48464937T>G , CM000675.2:g.48464937T>G | GRCh38 |
NC_000013.10:g.49039073T>G , CM000675.1:g.49039073T>G | GRCh37 |
NC_000013.9:g.47937074T>G | NCBI36 |
NG_009009.1:g.166191T>G , LRG_517:g.166191T>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000267163.6:c.2212-61T>G MANE Select | ENSP00000267163.4:n.2212-61T>G | |
ENST00000643064.1:c.194+83494T>G | ||
ENST00000650461.1:c.2212-61T>G | ENSP00000497193.1:n.2212-61T>G | |
ENST00000267163.4:c.2212-61T>G | ENSP00000267163.4:n.2212-61T>G | |
NM_000321.2:c.2212-61T>G , LRG_517t1:c.2212-61T>G | NP_000312.2:n.2212-61T>G | |
XM_011535171.1:c.1951-61T>G | XP_011533473.1:n.1951-61T>G | |
XM_011535171.2:c.1951-61T>G | XP_011533473.1:n.1951-61T>G | |
NM_000321.3:c.2212-61T>G MANE Select | NP_000312.2:n.2212-61T>G |