Linked Data
ClinVar Variation Id:
2027577
ClinVar RCV Id:
RCV002889507
gnomAD v4:
16-28932940-C-T
MyVariant Identifiers:
chr16:g.28944261C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.28932940C>T , CM000678.2:g.28932940C>T | GRCh38 |
| NC_000016.9:g.28944261C>T , CM000678.1:g.28944261C>T | GRCh37 |
| NC_000016.8:g.28851762C>T | NCBI36 |
| NG_007275.1:g.6002C>T , LRG_35:g.6002C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000324662.8:c.385C>T (CD19) | ENSP00000313419.4:p.Leu129= | |
| ENST00000538922.8:c.385C>T (CD19) MANE Select | ENSP00000437940.2:p.Leu129= | |
| ENST00000324662.7:c.385C>T (CD19) | ENSP00000313419.3:p.Leu129= | |
| ENST00000538922.5:c.385C>T (CD19) | ENSP00000437940.1:p.Leu129= | |
| ENST00000565089.5:n.719C>T (CD19) | ||
| ENST00000566762.1:c.-150+3324G>A (RABEP2) | ENSP00000454974.1:n.-150+3324G>A | |
| ENST00000566890.1:n.8C>T (CD19) | ||
| ENST00000567541.5:c.385C>T (CD19) | ENSP00000456201.1:p.Leu129= | |
| ENST00000611258.4:c.385C>T (CD19) | ENSP00000481090.1:p.Leu129= | |
| NM_001178098.1:c.385C>T (CD19) | NP_001171569.1:p.Leu129= | |
| NM_001770.5:c.385C>T , LRG_35t1:c.385C>T (CD19) | NP_001761.3:p.Leu129= | |
| XM_006721103.2:c.118C>T (CD19) | XP_006721166.1:p.Leu40= | |
| XM_011545981.1:c.385C>T (CD19) | XP_011544283.1:p.Leu129= | |
| XR_950871.1:n.447C>T (CD19) | ||
| XR_950872.1:n.447C>T (CD19) | ||
| XM_006721103.3:c.118C>T (CD19) | XP_006721166.1:p.Leu40= | |
| XM_011545981.2:c.385C>T (CD19) | XP_011544283.1:p.Leu129= | |
| XM_017023893.1:c.118C>T (CD19) | XP_016879382.1:p.Leu40= | |
| XR_950871.2:n.430C>T (CD19) | ||
| NM_001178098.2:c.385C>T (CD19) | NP_001171569.1:p.Leu129= | |
| NM_001770.6:c.385C>T (CD19) MANE Select | NP_001761.3:p.Leu129= | |
| NM_001385732.1:c.118C>T (CD19) | NP_001372661.1:p.Leu40= | |
| NR_169755.1:n.713C>T (CD19) |