Canonical Allele Identifier: CA2959756

Gene: ALB

Linked Data

• ClinVar Variation Id: 349641
• ClinVar RCV Id: RCV000324561
• dbSNP Id: rs746946403
• ExAC: 4:74286029 A / C
• gnomAD v2: 4-74286029-A-C
• gnomAD v3: 4-73420312-A-C
• gnomAD v4: 4-73420312-A-C
• MyVariant Identifiers: chr4:g.74286029A>C (hg19) ; chr4:g.73420312A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73420312A>C , CM000666.2:g.73420312A>C	GRCh38
NC_000004.11:g.74286029A>C , CM000666.1:g.74286029A>C	GRCh37
NC_000004.10:g.74504893A>C	NCBI36
NG_009291.1:g.21058A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.*14A>C MANE Select	ENSP00000295897.4:n.*14A>C
ENST00000295897.8:c.*14A>C	ENSP00000295897.4:n.*14A>C
ENST00000401494.7:c.*14A>C	ENSP00000384695.3:n.*14A>C
ENST00000415165.6:c.*14A>C	ENSP00000401820.2:n.*14A>C
ENST00000476441.6:c.*1123A>C	ENSP00000423727.1:n.*1123A>C
ENST00000495173.1:n.152A>C
ENST00000503124.5:c.*14A>C	ENSP00000421027.1:n.*14A>C
ENST00000505649.5:n.1391A>C
ENST00000508932.5:n.234A>C
ENST00000509063.5:c.1785+673A>C	ENSP00000422784.1:n.1785+673A>C
ENST00000511370.1:c.1377A>C
ENST00000621085.4:c.*14A>C	ENSP00000483421.1:n.*14A>C
ENST00000621628.4:c.*14A>C	ENSP00000480485.1:n.*14A>C
NM_000477.5:c.*14A>C	NP_000468.1:n.*14A>C
NM_000477.6:c.*14A>C	NP_000468.1:n.*14A>C
NM_000477.7:c.*14A>C MANE Select	NP_000468.1:n.*14A>C