Canonical Allele Identifier: CA3937466
Gene: ASCC3 HGNC NCBI

Linked Data

dbSNP Id: rs240768

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.100509468T>C , CM000668.2:g.100509468T>C GRCh38
NC_000006.11:g.100957344T>C , CM000668.1:g.100957344T>C GRCh37
NC_000006.10:g.101064065T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000369162.7:c.6527A>G MANE Select ENSP00000358159.2:p.Tyr2176Cys
ENST00000369162.6:c.6527A>G ENSP00000358159.2:p.Tyr2176Cys
ENST00000518006.1:n.443A>G
NM_006828.3:c.6527A>G NP_006819.2:p.Tyr2176Cys
XM_011535394.1:c.6542A>G XP_011533696.1:p.Tyr2181Cys
XM_011535395.1:c.6233A>G XP_011533697.1:p.Tyr2078Cys
XM_011535396.1:c.6233A>G XP_011533698.1:p.Tyr2078Cys
XM_011535394.3:c.6542A>G XP_011533696.1:p.Tyr2181Cys
XM_011535395.3:c.6233A>G XP_011533697.1:p.Tyr2078Cys
XM_011535396.3:c.6233A>G XP_011533698.1:p.Tyr2078Cys
XM_017010205.2:c.6233A>G XP_016865694.1:p.Tyr2078Cys
XM_017010206.2:c.5108A>G XP_016865695.1:p.Tyr1703Cys
XM_024446316.1:c.5729A>G XP_024302084.1:p.Tyr1910Cys
NM_006828.4:c.6527A>G MANE Select NP_006819.2:p.Tyr2176Cys