Canonical Allele Identifier: CA270573246

Gene: CYP19A1

Linked Data

• dbSNP Id: rs75940703
• MyVariant Identifiers: chr15:g.51630753C>G (hg19) ; chr15:g.51338556C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.51338556C>G , CM000677.2:g.51338556C>G	GRCh38
NC_000015.9:g.51630753C>G , CM000677.1:g.51630753C>G	GRCh37
NC_000015.8:g.49418045C>G	NCBI36
NG_007982.1:g.5043G>C
NG_054933.1:g.2041C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396402.6:c.-100G>C MANE Select	ENSP00000379683.1:n.-100G>C
ENST00000396402.5:c.-100G>C	ENSP00000379683.1:n.-100G>C
ENST00000396404.8:c.-209G>C	ENSP00000379685.4:n.-209G>C
ENST00000405011.6:c.-255G>C	ENSP00000384389.2:n.-255G>C
ENST00000439712.6:c.-344G>C	ENSP00000390614.2:n.-344G>C
ENST00000453807.6:c.-291G>C	ENSP00000391139.2:n.-291G>C
ENST00000492852.1:n.26G>C
ENST00000557858.5:c.-100G>C	ENSP00000452627.1:n.-100G>C
ENST00000557934.5:c.-100G>C	ENSP00000454004.1:n.-100G>C
ENST00000558328.5:c.-158G>C	ENSP00000453280.1:n.-158G>C
ENST00000559980.5:c.-435G>C	ENSP00000452872.1:n.-435G>C
ENST00000561075.5:c.-100G>C	ENSP00000454039.1:n.-100G>C
NM_000103.3:c.-100G>C	NP_000094.2:n.-100G>C
NM_031226.2:c.-209G>C	NP_112503.1:n.-209G>C
NM_000103.4:c.-100G>C MANE Select	NP_000094.2:n.-100G>C
NM_031226.3:c.-209G>C	NP_112503.1:n.-209G>C