Canonical Allele Identifier: CA2959757

Gene: ALB

Linked Data

• dbSNP Id: rs770788446
• ExAC: 4:74286030 G / C
• gnomAD v2: 4-74286030-G-C
• gnomAD v3: 4-73420313-G-C
• gnomAD v4: 4-73420313-G-C
• MyVariant Identifiers: chr4:g.74286030G>C (hg19) ; chr4:g.73420313G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73420313G>C , CM000666.2:g.73420313G>C	GRCh38
NC_000004.11:g.74286030G>C , CM000666.1:g.74286030G>C	GRCh37
NC_000004.10:g.74504894G>C	NCBI36
NG_009291.1:g.21059G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.*15G>C MANE Select	ENSP00000295897.4:n.*15G>C
ENST00000295897.8:c.*15G>C	ENSP00000295897.4:n.*15G>C
ENST00000401494.7:c.*15G>C	ENSP00000384695.3:n.*15G>C
ENST00000415165.6:c.*15G>C	ENSP00000401820.2:n.*15G>C
ENST00000476441.6:c.*1124G>C	ENSP00000423727.1:n.*1124G>C
ENST00000495173.1:n.153G>C
ENST00000503124.5:c.*15G>C	ENSP00000421027.1:n.*15G>C
ENST00000505649.5:n.1392G>C
ENST00000508932.5:n.235G>C
ENST00000509063.5:c.1785+674G>C	ENSP00000422784.1:n.1785+674G>C
ENST00000511370.1:c.1378G>C
ENST00000621085.4:c.*15G>C	ENSP00000483421.1:n.*15G>C
ENST00000621628.4:c.*15G>C	ENSP00000480485.1:n.*15G>C
NM_000477.5:c.*15G>C	NP_000468.1:n.*15G>C
NM_000477.6:c.*15G>C	NP_000468.1:n.*15G>C
NM_000477.7:c.*15G>C MANE Select	NP_000468.1:n.*15G>C