HGVS | Genome Assembly |
---|---|
NC_000009.12:g.134700037C>T , CM000671.2:g.134700037C>T | GRCh38 |
NC_000009.11:g.137591883C>T , CM000671.1:g.137591883C>T | GRCh37 |
NC_000009.10:g.136731704C>T | NCBI36 |
NG_008030.1:g.63232C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371820.4:c.406C>T | ENSP00000360885.4:p.Pro136Ser | |
ENST00000371817.8:c.406C>T MANE Select | ENSP00000360882.3:p.Pro136Ser | |
ENST00000371817.7:c.406C>T | ENSP00000360882.3:p.Pro136Ser | |
ENST00000464187.1:n.828C>T | ||
ENST00000618395.4:c.406C>T | ENSP00000481360.1:p.Pro136Ser | |
NM_000093.4:c.406C>T | NP_000084.3:p.Pro136Ser | |
NM_001278074.1:c.406C>T | NP_001265003.1:p.Pro136Ser | |
XR_929712.1:n.808C>T | ||
XR_929713.1:n.808C>T | ||
XM_017014266.2:c.406C>T | XP_016869755.1:p.Pro136Ser | |
XR_001746183.1:n.804C>T | ||
NM_000093.5:c.406C>T MANE Select | NP_000084.3:p.Pro136Ser |