Linked Data
gnomAD v2:
12-32977117-C-A
gnomAD v3:
12-32824183-C-A
gnomAD v4:
12-32824183-C-A
MyVariant Identifiers:
chr12:g.32977117_32977118delinsAA (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.32824183C>A , CM000674.2:g.32824183C>A | GRCh38 |
| NC_000012.11:g.32977117C>A , CM000674.1:g.32977117C>A | GRCh37 |
| NC_000012.10:g.32868384C>A | NCBI36 |
| NG_009000.1:g.77664G>T , LRG_398:g.77664G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000700555.2:n.69-21G>T | ||
| ENST00000700559.2:c.1557-21G>T | ENSP00000515065.2:n.1557-21G>T | |
| ENST00000700563.2:c.1557-21G>T | ENSP00000515066.2:n.1557-21G>T | |
| ENST00000546498.2:n.223G>T | ||
| ENST00000700555.1:c.-4-21G>T | ENSP00000515062.1:n.-4-21G>T | |
| ENST00000700556.1:c.28-21G>T | ||
| ENST00000700559.1:c.772-21G>T | ||
| ENST00000700560.1:n.772-21G>T | ||
| ENST00000700561.1:n.898-21G>T | ||
| ENST00000700563.1:c.1511-21G>T | ||
| ENST00000700564.1:n.1561-21G>T | ||
| ENST00000070846.11:c.1689-21G>T | ENSP00000070846.6:n.1689-21G>T | |
| ENST00000340811.9:c.1557-21G>T MANE Select | ENSP00000342800.5:n.1557-21G>T | |
| ENST00000070846.10:c.1689-21G>T | ENSP00000070846.6:n.1689-21G>T | |
| ENST00000340811.8:c.1557-21G>T | ENSP00000342800.4:n.1557-21G>T | |
| ENST00000546498.1:n.223G>T | ||
| ENST00000613243.1:c.1689-21G>T | ENSP00000478295.1:n.1689-21G>T | |
| NM_001005242.2:c.1557-21G>T | NP_001005242.2:n.1557-21G>T | |
| NM_004572.3:c.1689-21G>T , LRG_398t1:c.1689-21G>T | NP_004563.2:n.1689-21G>T | |
| NM_001005242.3:c.1557-21G>T MANE Select | NP_001005242.2:n.1557-21G>T | |
| NM_004572.4:c.1689-21G>T | NP_004563.2:n.1689-21G>T |