HGVS | Genome Assembly |
---|---|
NC_000006.12:g.24658472T>C , CM000668.2:g.24658472T>C | GRCh38 |
NC_000006.11:g.24658700T>C , CM000668.1:g.24658700T>C | GRCh37 |
NC_000006.10:g.24766679T>C | NCBI36 |
NG_052787.1:g.13416A>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000378198.9:c.425+89A>G MANE Select | ENSP00000367440.4:n.425+89A>G | |
ENST00000341060.3:c.251+89A>G | ENSP00000345345.3:n.251+89A>G | |
ENST00000378198.8:c.425+89A>G | ENSP00000367440.4:n.425+89A>G | |
ENST00000478285.1:n.612+89A>G | ||
ENST00000478507.1:n.320-5319A>G | ||
NM_016614.2:c.425+89A>G | NP_057698.2:n.425+89A>G | |
XR_926244.1:n.552+89A>G | ||
NM_016614.3:c.425+89A>G MANE Select | NP_057698.2:n.425+89A>G |