Linked Data
dbSNP Id:
rs2079540631
gnomAD v3:
2-71381892-C-T
gnomAD v4:
2-71381892-C-T
MyVariant Identifiers:
chr2:g.71609022C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.71381892C>T , CM000664.2:g.71381892C>T | GRCh38 |
| NC_000002.11:g.71609022C>T , CM000664.1:g.71609022C>T | GRCh37 |
| NC_000002.10:g.71462530C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000264447.9:c.2377+1327C>T MANE Select | ENSP00000264447.4:n.2377+1327C>T | |
| ENST00000264447.8:c.2377+1327C>T | ENSP00000264447.4:n.2377+1327C>T | |
| ENST00000409544.5:c.2377+1327C>T | ENSP00000386433.1:n.2377+1327C>T | |
| ENST00000410075.5:c.2377+1327C>T | ENSP00000485608.1:n.2377+1327C>T | |
| ENST00000491843.2:n.224+989C>T | ||
| NM_001014972.2:c.2377+1327C>T | NP_001014972.1:n.2377+1327C>T | |
| NM_001252612.1:c.2377+1327C>T | NP_001239541.1:n.2377+1327C>T | |
| NM_001252613.1:c.2377+1327C>T | NP_001239542.1:n.2377+1327C>T | |
| NM_014497.4:c.2377+1327C>T | NP_055312.2:n.2377+1327C>T | |
| XM_005264263.1:c.844+1327C>T | XP_005264320.1:n.844+1327C>T | |
| XM_006711989.1:c.844+1327C>T | XP_006712052.1:n.844+1327C>T | |
| XM_011532767.1:c.2377+1327C>T | XP_011531069.1:n.2377+1327C>T | |
| XM_011532768.1:c.2377+1327C>T | XP_011531070.1:n.2377+1327C>T | |
| XM_011532769.1:c.2377+1327C>T | XP_011531071.1:n.2377+1327C>T | |
| XR_939678.1:n.2492+1327C>T | ||
| XM_011532768.3:c.2695+1327C>T | XP_011531070.2:n.2695+1327C>T | |
| XM_017003809.2:c.2695+1327C>T | XP_016859298.1:n.2695+1327C>T | |
| XM_017003810.2:c.2377+1327C>T | XP_016859299.1:n.2377+1327C>T | |
| XM_017003812.2:c.2695+1327C>T | XP_016859301.1:n.2695+1327C>T | |
| XR_001738706.2:n.2741+1327C>T | ||
| XR_001738707.2:n.2679+1327C>T | ||
| XR_002959264.1:n.2741+1327C>T | ||
| XR_002959265.1:n.2741+1327C>T | ||
| XR_002959266.1:n.2741+1327C>T | ||
| XR_939678.3:n.2741+1327C>T | ||
| NM_014497.5:c.2377+1327C>T MANE Select | NP_055312.2:n.2377+1327C>T | |
| NM_001014972.3:c.2377+1327C>T | NP_001014972.1:n.2377+1327C>T | |
| NM_001252612.2:c.2377+1327C>T | NP_001239541.1:n.2377+1327C>T | |
| NM_001252613.2:c.2377+1327C>T | NP_001239542.1:n.2377+1327C>T |