Linked Data
dbSNP Id:
rs1301847347
gnomAD v2:
8-145744440-A-G
gnomAD v3:
8-144519056-A-G
gnomAD v4:
8-144519056-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.144519056A>G , CM000670.2:g.144519056A>G | GRCh38 |
| NC_000008.10:g.145744440A>G , CM000670.1:g.145744440A>G | GRCh37 |
| NC_000008.9:g.145715248A>G | NCBI36 |
| NG_016430.1:g.3771T>C | |
| NG_033083.1:g.6092A>G | |
| NG_016430.2:g.3771T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000292524.6:c.-111-559A>G MANE Select | ENSP00000292524.1:n.-111-559A>G | |
| ENST00000292524.5:c.-111-559A>G | ENSP00000292524.1:n.-111-559A>G | |
| ENST00000525766.1:c.-112+241A>G | ENSP00000434738.1:n.-112+241A>G | |
| ENST00000527730.1:c.-25-645A>G | ENSP00000436452.1:n.-25-645A>G | |
| ENST00000529022.5:c.-112+241A>G | ENSP00000434768.1:n.-112+241A>G | |
| ENST00000530854.1:c.-26+241A>G | ENSP00000435985.1:n.-26+241A>G | |
| NM_001272036.1:c.-112+241A>G | NP_001258965.1:n.-112+241A>G | |
| NM_014665.3:c.-111-559A>G | NP_055480.1:n.-111-559A>G | |
| XM_005272358.3:c.-25-645A>G | XP_005272415.1:n.-25-645A>G | |
| XM_005272359.3:c.-26+241A>G | XP_005272416.1:n.-26+241A>G | |
| XM_005272360.3:c.-9-778A>G | XP_005272417.1:n.-9-778A>G | |
| XM_005272361.2:c.-375-645A>G | XP_005272418.1:n.-375-645A>G | |
| XM_011517387.1:c.-552-118A>G | XP_011515689.1:n.-552-118A>G | |
| XM_011517388.1:c.-10+241A>G | XP_011515690.1:n.-10+241A>G | |
| XR_928369.1:n.121+241A>G | ||
| XR_928370.1:n.121+241A>G | ||
| XR_928371.1:n.121+241A>G | ||
| XM_005272358.5:c.-25-645A>G | XP_005272415.1:n.-25-645A>G | |
| XM_005272359.5:c.-26+241A>G | XP_005272416.1:n.-26+241A>G | |
| XM_005272360.5:c.-9-778A>G | XP_005272417.1:n.-9-778A>G | |
| XM_017014005.2:c.-10+241A>G | XP_016869494.1:n.-10+241A>G | |
| XM_024447336.1:c.-112+241A>G | XP_024303104.1:n.-112+241A>G | |
| XM_024447337.1:c.-10+241A>G | XP_024303105.1:n.-10+241A>G | |
| XM_024447338.1:c.-461-559A>G | XP_024303106.1:n.-461-559A>G | |
| XM_024447339.1:c.-375-645A>G | XP_024303107.1:n.-375-645A>G | |
| XM_024447340.1:c.-243+241A>G | XP_024303108.1:n.-243+241A>G | |
| XM_024447341.1:c.-242-778A>G | XP_024303109.1:n.-242-778A>G | |
| NM_014665.4:c.-111-559A>G MANE Select | NP_055480.1:n.-111-559A>G | |
| NM_001272036.2:c.-112+241A>G | NP_001258965.1:n.-112+241A>G |