Canonical Allele Identifier: CA1064142792

Gene: ALB

Linked Data

• dbSNP Id: rs1719112969
• gnomAD v3: 4-73420316-T-C
• gnomAD v4: 4-73420316-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73420316T>C , CM000666.2:g.73420316T>C	GRCh38
NC_000004.11:g.74286033T>C , CM000666.1:g.74286033T>C	GRCh37
NC_000004.10:g.74504897T>C	NCBI36
NG_009291.1:g.21062T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.*18T>C MANE Select	ENSP00000295897.4:n.*18T>C
ENST00000295897.8:c.*18T>C	ENSP00000295897.4:n.*18T>C
ENST00000401494.7:c.*18T>C	ENSP00000384695.3:n.*18T>C
ENST00000415165.6:c.*18T>C	ENSP00000401820.2:n.*18T>C
ENST00000476441.6:c.*1127T>C	ENSP00000423727.1:n.*1127T>C
ENST00000495173.1:n.156T>C
ENST00000503124.5:c.*18T>C	ENSP00000421027.1:n.*18T>C
ENST00000505649.5:n.1395T>C
ENST00000508932.5:n.238T>C
ENST00000509063.5:c.1785+677T>C	ENSP00000422784.1:n.1785+677T>C
ENST00000511370.1:c.1381T>C
ENST00000621085.4:c.*18T>C	ENSP00000483421.1:n.*18T>C
ENST00000621628.4:c.*18T>C	ENSP00000480485.1:n.*18T>C
NM_000477.5:c.*18T>C	NP_000468.1:n.*18T>C
NM_000477.6:c.*18T>C	NP_000468.1:n.*18T>C
NM_000477.7:c.*18T>C MANE Select	NP_000468.1:n.*18T>C