HGVS | Genome Assembly |
---|---|
NC_000006.12:g.52084911A>G , CM000668.2:g.52084911A>G | GRCh38 |
NC_000006.11:g.51949709A>G , CM000668.1:g.51949709A>G | GRCh37 |
NC_000006.10:g.52057668A>G | NCBI36 |
NG_008753.1:g.7715T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371117.8:c.23T>C MANE Select | ENSP00000360158.3:p.Leu8Pro | |
ENST00000340994.4:c.23T>C | ENSP00000341097.4:p.Leu8Pro | |
ENST00000371117.7:c.23T>C | ENSP00000360158.3:p.Leu8Pro | |
NM_138694.3:c.23T>C | NP_619639.3:p.Leu8Pro | |
NM_170724.2:c.23T>C | NP_733842.2:p.Leu8Pro | |
XM_011514679.1:c.23T>C | XP_011512981.1:p.Leu8Pro | |
XM_011514680.1:c.23T>C | XP_011512982.1:p.Leu8Pro | |
XM_011514681.1:c.23T>C | XP_011512983.1:p.Leu8Pro | |
XM_011514682.1:c.23T>C | XP_011512984.1:p.Leu8Pro | |
XM_011514683.1:c.23T>C | XP_011512985.1:p.Leu8Pro | |
XM_011514685.1:c.23T>C | XP_011512987.1:p.Leu8Pro | |
XM_011514686.1:c.23T>C | XP_011512988.1:p.Leu8Pro | |
XM_011514687.1:c.23T>C | XP_011512989.1:p.Leu8Pro | |
XM_011514688.1:c.23T>C | XP_011512990.1:p.Leu8Pro | |
XM_011514689.1:c.23T>C | XP_011512991.1:p.Leu8Pro | |
XM_011514680.3:c.23T>C | XP_011512982.1:p.Leu8Pro | |
XM_011514682.3:c.23T>C | XP_011512984.1:p.Leu8Pro | |
XM_011514683.3:c.23T>C | XP_011512985.1:p.Leu8Pro | |
XM_011514686.2:c.23T>C | XP_011512988.1:p.Leu8Pro | |
XM_011514688.2:c.23T>C | XP_011512990.1:p.Leu8Pro | |
XM_017010944.2:c.23T>C | XP_016866433.1:p.Leu8Pro | |
XM_017010945.2:c.23T>C | XP_016866434.1:p.Leu8Pro | |
XM_017010946.2:c.23T>C | XP_016866435.1:p.Leu8Pro | |
XM_017010947.2:c.23T>C | XP_016866436.1:p.Leu8Pro | |
XM_017010950.1:c.23T>C | XP_016866439.1:p.Leu8Pro | |
XM_017010951.1:c.23T>C | XP_016866440.1:p.Leu8Pro | |
XM_017010952.1:c.23T>C | XP_016866441.1:p.Leu8Pro | |
XR_001743469.1:n.299T>C | ||
NM_138694.4:c.23T>C MANE Select | NP_619639.3:p.Leu8Pro | |
NM_170724.3:c.23T>C | NP_733842.2:p.Leu8Pro |