Linked Data
gnomAD v4:
16-67940346-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.67940346C>T , CM000678.2:g.67940346C>T | GRCh38 |
| NC_000016.9:g.67974249C>T , CM000678.1:g.67974249C>T | GRCh37 |
| NC_000016.8:g.66531750C>T | NCBI36 |
| NG_009778.1:g.8767G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264005.10:c.881G>A MANE Select | ENSP00000264005.5:p.Ser294Asn | |
| ENST00000264005.9:c.881G>A | ENSP00000264005.5:p.Ser294Asn | |
| ENST00000570369.5:c.156-272G>A | ||
| ENST00000570980.1:c.665G>A | ENSP00000464651.1:p.Ser222Asn | |
| ENST00000573538.5:c.619G>A | ENSP00000463220.1:n.619G>A | |
| NM_000229.1:c.881G>A | NP_000220.1:p.Ser294Asn | |
| NM_000229.2:c.881G>A MANE Select | NP_000220.1:p.Ser294Asn |