Linked Data
MyVariant Identifiers:
chr6:g.31828347G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31860570G>A , CM000668.2:g.31860570G>A | GRCh38 |
| NC_000006.11:g.31828347G>A , CM000668.1:g.31828347G>A | GRCh37 |
| NC_000006.10:g.31936326G>A | NCBI36 |
| NG_008201.1:g.7363C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000375631.5:c.667C>T MANE Select | ENSP00000364782.4:p.Leu223= | |
| ENST00000677054.1:n.1910C>T | ||
| ENST00000677512.1:n.775C>T | ||
| ENST00000678869.1:n.1341C>T | ||
| ENST00000375631.4:c.667C>T | ENSP00000364782.4:p.Leu223= | |
| ENST00000480384.1:n.696C>T | ||
| ENST00000491768.5:c.667C>T | ENSP00000433127.1:p.Leu223= | |
| ENST00000495807.1:n.1801C>T | ||
| NM_000434.3:c.667C>T | NP_000425.1:p.Leu223= | |
| NM_000434.4:c.667C>T MANE Select | NP_000425.1:p.Leu223= |