Canonical Allele Identifier: CA566363990

Gene: APOM BAG6

Linked Data

• dbSNP Id: rs1458807981
• gnomAD v2: 6-31624787-G-T
• gnomAD v3: 6-31657010-G-T
• gnomAD v4: 6-31657010-G-T
• MyVariant Identifiers: chr6:g.31624787G>T (hg19) ; chr6:g.31657010G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31657010G>T , CM000668.2:g.31657010G>T	GRCh38
NC_000006.11:g.31624787G>T , CM000668.1:g.31624787G>T	GRCh37
NC_000006.10:g.31732766G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000375916.4:c.270-215G>T (APOM) MANE Select	ENSP00000365081.3:n.270-215G>T
ENST00000375916.3:c.270-215G>T (APOM)	ENSP00000365081.3:n.270-215G>T
ENST00000375918.6:c.54-215G>T (APOM)	ENSP00000365083.2:n.54-215G>T
ENST00000375920.8:c.54-215G>T (APOM)	ENSP00000365085.4:n.54-215G>T
NM_001256169.1:c.54-215G>T (APOM)	NP_001243098.1:n.54-215G>T
NM_019101.2:c.270-215G>T (APOM)	NP_061974.2:n.270-215G>T
NR_045828.1:n.305-215G>T (APOM)
XM_006715150.2:c.174-215G>T (APOM)	XP_006715213.1:n.174-215G>T
XM_011514895.1:c.-14+3311C>A (BAG6)	XP_011513197.1:n.-14+3311C>A
XM_006715150.3:c.174-215G>T (APOM)	XP_006715213.1:n.174-215G>T
XM_017011279.2:c.-14+3311C>A (BAG6)	XP_016866768.1:n.-14+3311C>A
XM_024446545.1:c.-14+754C>A (BAG6)	XP_024302313.1:n.-14+754C>A
NM_019101.3:c.270-215G>T (APOM) MANE Select	NP_061974.2:n.270-215G>T
NM_001256169.2:c.54-215G>T (APOM)	NP_001243098.1:n.54-215G>T
NR_045828.2:n.311-215G>T (APOM)