HGVS | Genome Assembly |
---|---|
NC_000009.12:g.134750808G= , CM000671.2:g.134750808G= | GRCh38 |
NC_000009.11:g.137642654G= , CM000671.1:g.137642654G= | GRCh37 |
NC_000009.10:g.136782475G= | NCBI36 |
NG_008030.1:g.114003G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371820.4:c.1588G= | ENSP00000360885.4:p.Gly530= | |
ENST00000371817.8:c.1588G= MANE Select | ENSP00000360882.3:p.Gly530= | |
ENST00000371817.7:c.1588G= | ENSP00000360882.3:p.Gly530= | |
ENST00000618395.4:c.1588G= | ENSP00000481360.1:p.Gly530= | |
NM_000093.4:c.1588G= | NP_000084.3:p.Gly530= | |
NM_001278074.1:c.1588G= | NP_001265003.1:p.Gly530= | |
XR_929712.1:n.1990G= | ||
XR_929713.1:n.1990G= | ||
XM_017014266.2:c.1588G= | XP_016869755.1:p.Gly530= | |
XR_001746183.1:n.1986G= | ||
NM_000093.5:c.1588G= MANE Select | NP_000084.3:p.Gly530= |