HGVS | Genome Assembly |
---|---|
NC_000019.10:g.45459513T>G , CM000681.2:g.45459513T>G | GRCh38 |
NC_000019.9:g.45962771T>G , CM000681.1:g.45962771T>G | GRCh37 |
NC_000019.8:g.50654611T>G | NCBI36 |
NG_015839.2:g.24316A>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000423698.6:c.-8+19223A>C | ENSP00000394875.2:n.-8+19223A>C | |
XM_005258636.3:c.-8+19223A>C | XP_005258693.1:n.-8+19223A>C | |
XM_005258636.4:c.-8+19223A>C | XP_005258693.1:n.-8+19223A>C | |
XM_017026464.1:c.-8+19223A>C | XP_016881953.1:n.-8+19223A>C |