Linked Data
dbSNP Id:
rs1344601525
gnomAD v2:
6-33132862-T-C
gnomAD v3:
6-33165085-T-C
gnomAD v4:
6-33165085-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.33165085T>C , CM000668.2:g.33165085T>C | GRCh38 |
| NC_000006.11:g.33132862T>C , CM000668.1:g.33132862T>C | GRCh37 |
| NC_000006.10:g.33240840T>C | NCBI36 |
| NG_011589.1:g.32384A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000683572.1:n.557-121A>G | ||
| ENST00000341947.7:c.4751-121A>G MANE Select | ENSP00000339915.2:n.4751-121A>G | |
| ENST00000341947.6:c.4751-121A>G | ENSP00000339915.2:n.4751-121A>G | |
| ENST00000361917.5:c.4430-121A>G | ENSP00000355123.1:n.4430-121A>G | |
| ENST00000374708.8:c.4493-121A>G | ENSP00000363840.4:n.4493-121A>G | |
| ENST00000477772.1:n.541-121A>G | ||
| NM_080679.2:c.4430-121A>G | NP_542410.2:n.4430-121A>G | |
| NM_080680.2:c.4751-121A>G | NP_542411.2:n.4751-121A>G | |
| NM_080681.2:c.4493-121A>G | NP_542412.2:n.4493-121A>G | |
| XM_011514298.1:c.3905-121A>G | XP_011512600.1:n.3905-121A>G | |
| XM_011514299.1:c.4037-121A>G | XP_011512601.1:n.4037-121A>G | |
| XM_011514300.1:c.3857-121A>G | XP_011512602.1:n.3857-121A>G | |
| XM_011514301.1:c.3794-121A>G | XP_011512603.1:n.3794-121A>G | |
| XM_011514302.1:c.3638-121A>G | XP_011512604.1:n.3638-121A>G | |
| XM_011514299.2:c.4037-121A>G | XP_011512601.1:n.4037-121A>G | |
| XM_011514300.2:c.3857-121A>G | XP_011512602.1:n.3857-121A>G | |
| XM_011514302.2:c.3638-121A>G | XP_011512604.1:n.3638-121A>G | |
| XM_017010250.1:c.4751-121A>G | XP_016865739.1:n.4751-121A>G | |
| XM_017010251.2:c.3569-121A>G | XP_016865740.1:n.3569-121A>G | |
| NM_080680.3:c.4751-121A>G MANE Select | NP_542411.2:n.4751-121A>G | |
| NM_080681.3:c.4493-121A>G | NP_542412.2:n.4493-121A>G | |
| NM_080679.3:c.4430-121A>G | NP_542410.2:n.4430-121A>G |