HGVS | Genome Assembly |
---|---|
NC_000010.11:g.131149699C>G , CM000672.2:g.131149699C>G | GRCh38 |
NC_000010.10:g.132947962C>G , CM000672.1:g.132947962C>G | GRCh37 |
NC_000010.9:g.132837952C>G | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000368642.4:c.1035-3039G>C MANE Select | ENSP00000357631.4:n.1035-3039G>C | |
ENST00000483040.1:n.2897-3039G>C | ||
NM_174937.3:c.1035-3039G>C | NP_777597.2:n.1035-3039G>C | |
XM_011539577.1:c.1074-3039G>C | XP_011537879.1:n.1074-3039G>C | |
NM_174937.4:c.1035-3039G>C MANE Select | NP_777597.2:n.1035-3039G>C |