HGVS | Genome Assembly |
---|---|
NC_000019.10:g.48750840C>A , CM000681.2:g.48750840C>A | GRCh38 |
NC_000019.9:g.49254097C>A , CM000681.1:g.49254097C>A | GRCh37 |
NC_000019.8:g.53945909C>A | NCBI36 |
NG_007510.1:g.9551G>T | |
NG_007510.2:g.9551G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000645652.2:c.442G>T MANE Select | ENSP00000494643.1:p.Asp148Tyr | |
ENST00000310160.7:c.442G>T | ENSP00000312021.3:p.Asp148Tyr | |
NM_000148.3:c.442G>T | NP_000139.1:p.Asp148Tyr | |
XM_006723127.1:c.811G>T | XP_006723190.1:p.Asp271Tyr | |
NM_001329877.1:c.442G>T | NP_001316806.1:p.Asp148Tyr | |
NM_000148.4:c.442G>T | NP_000139.1:p.Asp148Tyr | |
NM_001384359.1:c.442G>T MANE Select | NP_001371288.1:p.Asp148Tyr |