MyVariant.info:
GRCh37
chr2:g.166615953A>G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.165759443A>G , CM000664.2:g.165759443A>G | GRCh38 |
| NC_000002.11:g.166615953A>G , CM000664.1:g.166615953A>G | GRCh37 |
| NC_000002.10:g.166324199A>G | NCBI36 |
| NG_012069.1:g.39851T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000392701.8:c.966T>C MANE Select | ENSP00000376465.3:p.Tyr322= | |
| ENST00000392701.7:c.966T>C | ENSP00000376465.3:p.Tyr322= | |
| ENST00000409882.5:c.180T>C | ENSP00000386955.1:p.Tyr60= | |
| ENST00000412248.5:c.966T>C | ENSP00000412643.1:p.Tyr322= | |
| ENST00000437849.1:c.394T>C | ENSP00000391104.1:n.394T>C | |
| ENST00000463254.1:n.249T>C | ||
| NM_004482.3:c.966T>C | NP_004473.2:p.Tyr322= | |
| XM_005246449.1:c.966T>C | XP_005246506.1:p.Tyr322= | |
| XM_006712402.2:c.966T>C | XP_006712465.1:p.Tyr322= | |
| XM_011510929.1:c.966T>C | XP_011509231.1:p.Tyr322= | |
| XM_017003770.1:c.966T>C | XP_016859259.1:p.Tyr322= | |
| XR_002959253.1:n.1307T>C | ||
| NM_004482.4:c.966T>C MANE Select | NP_004473.2:p.Tyr322= |