HGVS | Genome Assembly |
---|---|
NC_000005.10:g.34008060T>C , CM000667.2:g.34008060T>C | GRCh38 |
NC_000005.9:g.34008165T>C , CM000667.1:g.34008165T>C | GRCh37 |
NC_000005.8:g.34043922T>C | NCBI36 |
NG_016211.1:g.5056A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000335606.10:c.-41A>G (AMACR) | ENSP00000334424.6:n.-41A>G | |
ENST00000382079.3:c.690-2161A>G (C1QTNF3-AMACR) | ENSP00000371511.3:n.690-2161A>G | |
ENST00000426255.6:c.-41A>G (AMACR) | ENSP00000476965.1:n.-41A>G | |
ENST00000502637.5:c.-41A>G (AMACR) | ENSP00000424351.1:n.-41A>G | |
NM_001167595.1:c.-41A>G (AMACR) | NP_001161067.1:n.-41A>G | |
NM_014324.5:c.-41A>G (AMACR) | NP_055139.4:n.-41A>G | |
NM_203382.2:c.-41A>G (AMACR) | NP_976316.1:n.-41A>G | |
NR_037951.1:n.765-2161A>G (C1QTNF3-AMACR) |