HGVS | Genome Assembly |
---|---|
NC_000009.12:g.130862867A>C , CM000671.2:g.130862867A>C | GRCh38 |
NC_000009.11:g.133738254A>C , CM000671.1:g.133738254A>C | GRCh37 |
NC_000009.10:g.132728075A>C | NCBI36 |
NG_012034.1:g.153987A>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000372348.9:c.711A>C | ENSP00000361423.2:p.Pro237= | |
ENST00000318560.6:c.654A>C MANE Select | ENSP00000323315.5:p.Pro218= | |
ENST00000372348.7:c.711A>C | ENSP00000361423.2:p.Pro237= | |
ENST00000318560.5:c.654A>C | ENSP00000323315.5:p.Pro218= | |
ENST00000372348.6:c.711A>C | ENSP00000361423.2:p.Pro237= | |
NM_005157.5:c.654A>C | NP_005148.2:p.Pro218= | |
NM_007313.2:c.711A>C | NP_009297.2:p.Pro237= | |
NM_005157.6:c.654A>C MANE Select | NP_005148.2:p.Pro218= | |
NM_007313.3:c.711A>C | NP_009297.2:p.Pro237= |