HGVS | Genome Assembly |
---|---|
NC_000002.12:g.135856590T>C , CM000664.2:g.135856590T>C | GRCh38 |
NC_000002.11:g.136614160T>C , CM000664.1:g.136614160T>C | GRCh37 |
NC_000002.10:g.136330630T>C | NCBI36 |
NG_008104.2:g.3580A>G , LRG_338:g.3580A>G | |
NG_008958.1:g.24852A>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000264156.3:c.1626+138A>G MANE Select | ENSP00000264156.2:n.1626+138A>G | |
ENST00000264156.2:c.1626+138A>G | ENSP00000264156.2:n.1626+138A>G | |
ENST00000492091.1:n.182-5027A>G | ||
NM_005915.5:c.1626+138A>G | NP_005906.2:n.1626+138A>G | |
NM_005915.6:c.1626+138A>G MANE Select | NP_005906.2:n.1626+138A>G |