HGVS | Genome Assembly |
---|---|
NC_000015.10:g.48489934T>G , CM000677.2:g.48489934T>G | GRCh38 |
NC_000015.9:g.48782131T>G , CM000677.1:g.48782131T>G | GRCh37 |
NC_000015.8:g.46569423T>G | NCBI36 |
NG_008805.2:g.160855A>C , LRG_778:g.160855A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000559133.6:c.2999A>C | ENSP00000453958.2:p.Asn1000Thr | |
ENST00000674301.2:c.2999A>C | ENSP00000501333.2:p.Asn1000Thr | |
ENST00000684448.1:n.1673A>C | ||
ENST00000316623.10:c.2999A>C MANE Select | ENSP00000325527.5:p.Asn1000Thr | |
ENST00000316623.9:c.2999A>C | ENSP00000325527.5:p.Asn1000Thr | |
ENST00000537463.6:c.637-15284A>C | ENSP00000440294.2:n.637-15284A>C | |
NM_000138.4:c.2999A>C , LRG_778t1:c.2999A>C | NP_000129.3:p.Asn1000Thr | |
NM_000138.5:c.2999A>C MANE Select | NP_000129.3:p.Asn1000Thr |