MyVariant.info:
GRCh37
chr13:g.23913263G>A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.23339124G>A , CM000675.2:g.23339124G>A | GRCh38 |
| NC_000013.10:g.23913263G>A , CM000675.1:g.23913263G>A | GRCh37 |
| NC_000013.9:g.22811263G>A | NCBI36 |
| NG_012342.1:g.99579C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682775.1:c.2185+14661C>T | ENSP00000508399.1:n.2185+14661C>T | |
| ENST00000682944.1:c.4779C>T | ENSP00000507173.1:p.Asn1593= | |
| ENST00000683210.1:c.2185+14661C>T | ENSP00000506739.1:n.2185+14661C>T | |
| ENST00000683270.1:c.4743C>T | ENSP00000507624.1:p.Asn1581= | |
| ENST00000683367.1:c.2177-9640C>T | ENSP00000507780.1:n.2177-9640C>T | |
| ENST00000683489.1:c.2291+2461C>T | ENSP00000508403.1:n.2291+2461C>T | |
| ENST00000683680.1:c.2318+2461C>T | ENSP00000507223.1:n.2318+2461C>T | |
| ENST00000684163.1:c.2203+7687C>T | ENSP00000508262.1:n.2203+7687C>T | |
| ENST00000684196.1:n.4543-9640C>T | ||
| ENST00000684325.1:c.2185+14661C>T | ENSP00000508121.1:n.2185+14661C>T | |
| ENST00000684385.1:c.2220+7687C>T | ENSP00000507855.1:n.2220+7687C>T | |
| ENST00000684497.1:c.2185+14661C>T | ENSP00000507057.1:n.2185+14661C>T | |
| ENST00000382292.9:c.4752C>T MANE Select | ENSP00000371729.3:p.Asn1584= | |
| ENST00000423156.2:c.2186-9640C>T | ENSP00000390925.2:n.2186-9640C>T | |
| ENST00000455470.6:c.2431+2321C>T | ENSP00000406565.2:n.2431+2321C>T | |
| ENST00000382292.7:c.4752C>T | ENSP00000371729.3:p.Asn1584= | |
| ENST00000382298.7:c.4752C>T | ENSP00000371735.3:p.Asn1584= | |
| ENST00000402364.1:c.2502C>T | ENSP00000385844.1:p.Asn834= | |
| ENST00000423156.1:c.1058-9640C>T | ENSP00000390925.1:n.1058-9640C>T | |
| ENST00000455470.5:c.2129+2321C>T | ||
| NM_001278055.1:c.4311C>T | NP_001264984.1:p.Asn1437= | |
| NM_014363.5:c.4752C>T | NP_055178.3:p.Asn1584= | |
| XM_005266338.1:c.4779C>T | XP_005266395.1:p.Asn1593= | |
| XM_011535038.1:c.4803C>T | XP_011533340.1:p.Asn1601= | |
| XM_011535039.1:c.4770C>T | XP_011533341.1:p.Asn1590= | |
| XM_005266338.2:c.4779C>T | XP_005266395.1:p.Asn1593= | |
| XM_011535039.2:c.4770C>T | XP_011533341.1:p.Asn1590= | |
| XM_017020539.1:c.4743C>T | XP_016876028.1:p.Asn1581= | |
| XM_024449337.1:c.4779C>T | XP_024305105.1:p.Asn1593= | |
| NM_014363.6:c.4752C>T MANE Select | NP_055178.3:p.Asn1584= | |
| NM_001278055.2:c.4311C>T | NP_001264984.1:p.Asn1437= |