Canonical Allele Identifier: CA718549406

Gene: ABCC6

Linked Data

• dbSNP Id: rs1486707301
• gnomAD v4: 16-16155245-C-T
• MyVariant Identifiers: chr16:g.16249102C>T (hg19) ; chr16:g.16155245C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16155245C>T , CM000678.2:g.16155245C>T	GRCh38
NC_000016.9:g.16249102C>T , CM000678.1:g.16249102C>T	GRCh37
NC_000016.8:g.16156603C>T	NCBI36
NG_007558.2:g.73227G>A
NG_007558.3:g.73373G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000576204.6:n.532G>A
ENST00000622290.5:c.*55-214G>A	ENSP00000483331.2:n.*55-214G>A
ENST00000205557.12:c.3883-214G>A MANE Select	ENSP00000205557.7:n.3883-214G>A
ENST00000640696.1:c.697-214G>A	ENSP00000492197.1:n.697-214G>A
ENST00000205557.11:c.3883-214G>A	ENSP00000205557.7:n.3883-214G>A
ENST00000456970.6:c.3508-214G>A	ENSP00000405002.2:n.3508-214G>A
ENST00000576204.5:n.532G>A
ENST00000622290.4:c.*1092-214G>A	ENSP00000483331.1:n.*1092-214G>A
NM_001171.5:c.3883-214G>A	NP_001162.4:n.3883-214G>A
XM_011522479.1:c.3850-214G>A	XP_011520781.1:n.3850-214G>A
XM_011522480.1:c.3541-214G>A	XP_011520782.1:n.3541-214G>A
XM_011522481.1:c.3541-214G>A	XP_011520783.1:n.3541-214G>A
XR_932836.1:n.4181-214G>A
XR_932837.1:n.3919-214G>A
XR_932838.1:n.3982-214G>A
XR_933134.1:n.539-4536C>T
NM_001351800.1:c.3541-214G>A	NP_001338729.1:n.3541-214G>A
NR_147784.1:n.3545-214G>A
XM_011522479.2:c.3850-214G>A	XP_011520781.1:n.3850-214G>A
XM_011522481.3:c.3541-214G>A	XP_011520783.1:n.3541-214G>A
XM_017023212.1:c.3715-214G>A	XP_016878701.1:n.3715-214G>A
XM_024450261.1:c.3919-214G>A	XP_024306029.1:n.3919-214G>A
XR_932836.2:n.4127-214G>A
XR_932837.3:n.3864-214G>A
XR_932838.3:n.3927-214G>A
NM_001171.6:c.3883-214G>A MANE Select	NP_001162.5:n.3883-214G>A