Canonical Allele Identifier: CA350586398

Gene: CYP27A1

Linked Data

• MyVariant Identifiers: chr2:g.219677337A>T (hg19) ; chr2:g.218812614A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218812614A>T , CM000664.2:g.218812614A>T	GRCh38
NC_000002.11:g.219677337A>T , CM000664.1:g.219677337A>T	GRCh37
NC_000002.10:g.219385581A>T	NCBI36
NG_007959.1:g.35866A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258415.9:c.709A>T MANE Select	ENSP00000258415.4:p.Thr237Ser
ENST00000258415.8:c.709A>T	ENSP00000258415.4:p.Thr237Ser
ENST00000411688.1:c.427A>T	ENSP00000392671.1:p.Thr143Ser
ENST00000445971.1:c.*170A>T	ENSP00000404945.1:n.*170A>T
ENST00000466602.1:n.657A>T
ENST00000494263.5:n.1143A>T
NM_000784.3:c.709A>T	NP_000775.1:p.Thr237Ser
XM_017003488.2:c.289A>T	XP_016858977.1:p.Thr97Ser
NM_000784.4:c.709A>T MANE Select	NP_000775.1:p.Thr237Ser