Canonical Allele Identifier: CA939372748
Gene: DHCR7 HGNC NCBI

Linked Data

dbSNP Id: rs1949287304

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.71436838C>G , CM000673.2:g.71436838C>G GRCh38
NC_000011.9:g.71147884C>G , CM000673.1:g.71147884C>G GRCh37
NC_000011.8:g.70825532C>G NCBI36
NG_012655.2:g.16594G>C , LRG_340:g.16594G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000525346.6:c.963+974G>C ENSP00000435707.3:n.963+974G>C
ENST00000526780.6:c.963+974G>C ENSP00000435668.2:n.963+974G>C
ENST00000527316.6:c.789+974G>C ENSP00000435047.2:n.789+974G>C
ENST00000682708.1:c.1014+974G>C ENSP00000506866.1:n.1014+974G>C
ENST00000682880.1:c.*836G>C ENSP00000507520.1:n.*836G>C
ENST00000683287.1:c.999+974G>C ENSP00000507607.1:n.999+974G>C
ENST00000683714.1:c.971+966G>C ENSP00000508207.1:n.971+966G>C
ENST00000684396.1:n.1003+974G>C
ENST00000685320.1:c.378+974G>C ENSP00000509319.1:n.378+974G>C
ENST00000690257.1:c.867+974G>C ENSP00000510750.1:n.867+974G>C
ENST00000355527.8:c.963+974G>C MANE Select ENSP00000347717.4:n.963+974G>C
ENST00000355527.7:c.963+974G>C ENSP00000347717.3:n.963+974G>C
ENST00000407721.6:c.963+974G>C ENSP00000384739.2:n.963+974G>C
ENST00000525137.1:c.331-865G>C ENSP00000435956.1:n.331-865G>C
ENST00000533800.5:c.213+974G>C ENSP00000435011.1:n.213+974G>C
ENST00000534795.5:c.319+974G>C
NM_001163817.1:c.963+974G>C NP_001157289.1:n.963+974G>C
NM_001360.2:c.963+974G>C , LRG_340t1:c.963+974G>C NP_001351.2:n.963+974G>C
XM_011544777.1:c.964-865G>C XP_011543079.1:n.964-865G>C
XM_011544777.2:c.964-865G>C XP_011543079.1:n.964-865G>C
NM_001163817.2:c.963+974G>C NP_001157289.1:n.963+974G>C
NM_001360.3:c.963+974G>C MANE Select NP_001351.2:n.963+974G>C