HGVS | Genome Assembly |
---|---|
NC_000008.11:g.118110140C>G , CM000670.2:g.118110140C>G | GRCh38 |
NC_000008.10:g.119122379C>G , CM000670.1:g.119122379C>G | GRCh37 |
NC_000008.9:g.119191560C>G | NCBI36 |
NG_007455.2:g.6680G>C , LRG_493:g.6680G>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000378204.7:c.907G>C MANE Select | ENSP00000367446.3:p.Asp303His | |
ENST00000436216.2:c.275G>C | ||
ENST00000378204.6:c.907G>C | ENSP00000367446.2:p.Asp303His | |
ENST00000436216.1:c.275G>C | ||
ENST00000437196.1:c.73+834G>C | ENSP00000407299.1:n.73+834G>C | |
NM_000127.2:c.907G>C , LRG_493t1:c.907G>C | NP_000118.2:p.Asp303His | |
NM_000127.3:c.907G>C MANE Select | NP_000118.2:p.Asp303His |