HGVS | Genome Assembly |
---|---|
NC_000017.11:g.10409165C>T , CM000679.2:g.10409165C>T | GRCh38 |
NC_000017.10:g.10312482C>T , CM000679.1:g.10312482C>T | GRCh37 |
NC_000017.9:g.10253207C>T | NCBI36 |
NG_013015.1:g.17786G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000403437.2:c.1898-1G>A (MYH8) MANE Select | ENSP00000384330.2:n.1898-1G>A | |
NM_002472.2:c.1898-1G>A (MYH8) | NP_002463.2:n.1898-1G>A | |
NR_125367.1:n.167+2927C>T (MYHAS) | ||
XM_011523873.1:c.1898-1G>A (MYH8) | XP_011522175.1:n.1898-1G>A | |
XM_011523874.1:c.1898-1G>A (MYH8) | XP_011522176.1:n.1898-1G>A | |
NM_002472.3:c.1898-1G>A (MYH8) MANE Select | NP_002463.2:n.1898-1G>A |