Canonical Allele Identifier: CA2656993885

Gene: SREBF2

Linked Data

• gnomAD v4: 22-41880565-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.41880565T>C , CM000684.2:g.41880565T>C	GRCh38
NC_000022.10:g.42276569T>C , CM000684.1:g.42276569T>C	GRCh37
NC_000022.9:g.40606515T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710853.1:c.1672-151T>C	ENSP00000518526.1:n.1672-151T>C
ENST00000361204.9:c.1762-151T>C MANE Select	ENSP00000354476.4:n.1762-151T>C
ENST00000361204.8:c.1762-151T>C	ENSP00000354476.4:n.1762-151T>C
ENST00000424354.5:c.1862-151T>C	ENSP00000395728.1:n.1862-151T>C
ENST00000612482.4:c.1772-151T>C	ENSP00000484441.1:n.1772-151T>C
NM_004599.3:c.1762-151T>C	NP_004590.2:n.1762-151T>C
NR_103834.1:n.2054-151T>C
XM_006724310.1:c.1672-151T>C	XP_006724373.1:n.1672-151T>C
XM_011530347.1:c.1387-151T>C	XP_011528649.1:n.1387-151T>C
XM_006724310.3:c.1672-151T>C	XP_006724373.1:n.1672-151T>C
XM_011530347.2:c.1387-151T>C	XP_011528649.1:n.1387-151T>C
XM_017028921.2:c.1762-151T>C	XP_016884410.1:n.1762-151T>C
XM_017028922.2:c.1762-151T>C	XP_016884411.1:n.1762-151T>C
XR_001755276.2:n.1905-151T>C
XR_001755277.2:n.1905-151T>C
XR_001755278.2:n.2028-151T>C
NM_004599.4:c.1762-151T>C MANE Select	NP_004590.2:n.1762-151T>C
NR_103834.2:n.2028-151T>C