Canonical Allele Identifier: CA411760785

Gene: SREBF2

Linked Data

• MyVariant Identifiers: chr22:g.42276762G>C (hg19) ; chr22:g.41880758G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.41880758G>C , CM000684.2:g.41880758G>C	GRCh38
NC_000022.10:g.42276762G>C , CM000684.1:g.42276762G>C	GRCh37
NC_000022.9:g.40606708G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710853.1:c.1714G>C	ENSP00000518526.1:p.Ala572Pro
ENST00000361204.9:c.1804G>C MANE Select	ENSP00000354476.4:p.Ala602Pro
ENST00000361204.8:c.1804G>C	ENSP00000354476.4:p.Ala602Pro
ENST00000424354.5:c.1904G>C	ENSP00000395728.1:p.Gly635Ala
ENST00000612482.4:c.1814G>C	ENSP00000484441.1:p.Gly605Ala
NM_004599.3:c.1804G>C	NP_004590.2:p.Ala602Pro
NR_103834.1:n.2096G>C
XM_006724310.1:c.1714G>C	XP_006724373.1:p.Ala572Pro
XM_011530347.1:c.1429G>C	XP_011528649.1:p.Ala477Pro
XM_006724310.3:c.1714G>C	XP_006724373.1:p.Ala572Pro
XM_011530347.2:c.1429G>C	XP_011528649.1:p.Ala477Pro
XM_017028921.2:c.1804G>C	XP_016884410.1:p.Ala602Pro
XM_017028922.2:c.1804G>C	XP_016884411.1:p.Ala602Pro
XR_001755276.2:n.1947G>C
XR_001755277.2:n.1947G>C
XR_001755278.2:n.2070G>C
NM_004599.4:c.1804G>C MANE Select	NP_004590.2:p.Ala602Pro
NR_103834.2:n.2070G>C