Canonical Allele Identifier: CA552307201

Gene: ALB

Linked Data

• dbSNP Id: rs1301517201
• gnomAD v2: 4-74285726-T-C
• gnomAD v3: 4-73420009-T-C
• gnomAD v4: 4-73420009-T-C
• MyVariant Identifiers: chr4:g.74285726T>C (hg19) ; chr4:g.73420009T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73420009T>C , CM000666.2:g.73420009T>C	GRCh38
NC_000004.11:g.74285726T>C , CM000666.1:g.74285726T>C	GRCh37
NC_000004.10:g.74504590T>C	NCBI36
NG_009291.1:g.20755T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1786-245T>C MANE Select	ENSP00000295897.4:n.1786-245T>C
ENST00000295897.8:c.1786-245T>C	ENSP00000295897.4:n.1786-245T>C
ENST00000401494.7:c.1441-245T>C	ENSP00000384695.3:n.1441-245T>C
ENST00000415165.6:c.1210-245T>C	ENSP00000401820.2:n.1210-245T>C
ENST00000476441.6:c.*1065-245T>C	ENSP00000423727.1:n.*1065-245T>C
ENST00000495173.1:n.94-245T>C
ENST00000503124.5:c.1336-245T>C	ENSP00000421027.1:n.1336-245T>C
ENST00000505649.5:n.1333-245T>C
ENST00000508932.5:n.176-245T>C
ENST00000509063.5:c.1785+370T>C	ENSP00000422784.1:n.1785+370T>C
ENST00000511370.1:c.1319-245T>C
ENST00000621085.4:c.1147-245T>C	ENSP00000483421.1:n.1147-245T>C
ENST00000621628.4:c.1147-245T>C	ENSP00000480485.1:n.1147-245T>C
NM_000477.5:c.1786-245T>C	NP_000468.1:n.1786-245T>C
NM_000477.6:c.1786-245T>C	NP_000468.1:n.1786-245T>C
NM_000477.7:c.1786-245T>C MANE Select	NP_000468.1:n.1786-245T>C