HGVS | Genome Assembly |
---|---|
NC_000001.11:g.173903977G>C , CM000663.2:g.173903977G>C | GRCh38 |
NC_000001.10:g.173873115G>C , CM000663.1:g.173873115G>C | GRCh37 |
NC_000001.9:g.172139738G>C | NCBI36 |
NG_012462.1:g.18402C>G , LRG_577:g.18402C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367698.4:c.1307C>G MANE Select | ENSP00000356671.3:p.Ala436Gly | |
ENST00000367698.3:c.1307C>G | ENSP00000356671.3:p.Ala436Gly | |
ENST00000617423.4:c.692C>G | ENSP00000478688.1:p.Ala231Gly | |
NM_000488.3:c.1307C>G , LRG_577t1:c.1307C>G | NP_000479.1:p.Ala436Gly | |
XM_005245198.2:c.1163C>G | XP_005245255.1:p.Ala388Gly | |
NM_001365052.1:c.1163C>G | NP_001351981.1:p.Ala388Gly | |
NM_000488.4:c.1307C>G MANE Select | NP_000479.1:p.Ala436Gly | |
NM_001365052.2:c.1163C>G | NP_001351981.1:p.Ala388Gly | |
NM_001386302.1:c.1430C>G | NP_001373231.1:p.Ala477Gly | |
NM_001386303.1:c.1388C>G | NP_001373232.1:p.Ala463Gly | |
NM_001386304.1:c.1286C>G | NP_001373233.1:p.Ala429Gly | |
NM_001386305.1:c.1250C>G | NP_001373234.1:p.Ala417Gly | |
NM_001386306.1:c.1091C>G | NP_001373235.1:p.Ala364Gly |