Canonical Allele Identifier: CA2670966758

Gene: ALB

Linked Data

• gnomAD v4: 4-73420232-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73420232T>C , CM000666.2:g.73420232T>C	GRCh38
NC_000004.11:g.74285949T>C , CM000666.1:g.74285949T>C	GRCh37
NC_000004.10:g.74504813T>C	NCBI36
NG_009291.1:g.20978T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1786-22T>C MANE Select	ENSP00000295897.4:n.1786-22T>C
ENST00000295897.8:c.1786-22T>C	ENSP00000295897.4:n.1786-22T>C
ENST00000401494.7:c.1441-22T>C	ENSP00000384695.3:n.1441-22T>C
ENST00000415165.6:c.1210-22T>C	ENSP00000401820.2:n.1210-22T>C
ENST00000476441.6:c.*1065-22T>C	ENSP00000423727.1:n.*1065-22T>C
ENST00000495173.1:n.94-22T>C
ENST00000503124.5:c.1336-22T>C	ENSP00000421027.1:n.1336-22T>C
ENST00000505649.5:n.1333-22T>C
ENST00000508932.5:n.176-22T>C
ENST00000509063.5:c.1785+593T>C	ENSP00000422784.1:n.1785+593T>C
ENST00000511370.1:c.1319-22T>C
ENST00000621085.4:c.1147-22T>C	ENSP00000483421.1:n.1147-22T>C
ENST00000621628.4:c.1147-22T>C	ENSP00000480485.1:n.1147-22T>C
NM_000477.5:c.1786-22T>C	NP_000468.1:n.1786-22T>C
NM_000477.6:c.1786-22T>C	NP_000468.1:n.1786-22T>C
NM_000477.7:c.1786-22T>C MANE Select	NP_000468.1:n.1786-22T>C