Linked Data
MyVariant Identifiers:
chr13:g.48955450T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.48381314T>C , CM000675.2:g.48381314T>C | GRCh38 |
| NC_000013.10:g.48955450T>C , CM000675.1:g.48955450T>C | GRCh37 |
| NC_000013.9:g.47853451T>C | NCBI36 |
| NG_009009.1:g.82568T>C , LRG_517:g.82568T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000267163.6:c.1566T>C MANE Select | ENSP00000267163.4:p.Asn522= | |
| ENST00000643064.1:c.65T>C | ||
| ENST00000650461.1:c.1566T>C | ENSP00000497193.1:p.Asn522= | |
| ENST00000267163.4:c.1566T>C | ENSP00000267163.4:p.Asn522= | |
| NM_000321.2:c.1566T>C , LRG_517t1:c.1566T>C | NP_000312.2:p.Asn522= | |
| XM_011535171.1:c.1305T>C | XP_011533473.1:p.Asn435= | |
| XM_011535171.2:c.1305T>C | XP_011533473.1:p.Asn435= | |
| NM_000321.3:c.1566T>C MANE Select | NP_000312.2:p.Asn522= |