Canonical Allele Identifier: CA2959660

Gene: ALB

Linked Data

• ClinVar Variation Id: 349631
• ClinVar RCV Id: RCV000399258
• dbSNP Id: rs373682659
• ExAC: 4:74283796 G / T
• gnomAD v2: 4-74283796-G-T
• gnomAD v3: 4-73418079-G-T
• gnomAD v4: 4-73418079-G-T
• MyVariant Identifiers: chr4:g.74283796G>T (hg19) ; chr4:g.73418079G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73418079G>T , CM000666.2:g.73418079G>T	GRCh38
NC_000004.11:g.74283796G>T , CM000666.1:g.74283796G>T	GRCh37
NC_000004.10:g.74502660G>T	NCBI36
NG_009291.1:g.18825G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1429-9G>T MANE Select	ENSP00000295897.4:n.1429-9G>T
ENST00000295897.8:c.1429-9G>T	ENSP00000295897.4:n.1429-9G>T
ENST00000401494.7:c.1084-9G>T	ENSP00000384695.3:n.1084-9G>T
ENST00000415165.6:c.853-9G>T	ENSP00000401820.2:n.853-9G>T
ENST00000476441.6:c.*708-9G>T	ENSP00000423727.1:n.*708-9G>T
ENST00000486939.1:n.74G>T
ENST00000503124.5:c.979-9G>T	ENSP00000421027.1:n.979-9G>T
ENST00000505649.5:n.976-9G>T
ENST00000509063.5:c.1429-9G>T	ENSP00000422784.1:n.1429-9G>T
ENST00000511370.1:c.962-9G>T
ENST00000621085.4:c.790-9G>T	ENSP00000483421.1:n.790-9G>T
ENST00000621628.4:c.790-9G>T	ENSP00000480485.1:n.790-9G>T
NM_000477.5:c.1429-9G>T	NP_000468.1:n.1429-9G>T
NM_000477.6:c.1429-9G>T	NP_000468.1:n.1429-9G>T
NM_000477.7:c.1429-9G>T MANE Select	NP_000468.1:n.1429-9G>T