Canonical Allele Identifier: CA357246111

Gene: ALB

Linked Data

• dbSNP Id: rs1719094758
• gnomAD v3: 4-73419530-A-C
• gnomAD v4: 4-73419530-A-C
• MyVariant Identifiers: chr4:g.74285247A>C (hg19) ; chr4:g.73419530A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73419530A>C , CM000666.2:g.73419530A>C	GRCh38
NC_000004.11:g.74285247A>C , CM000666.1:g.74285247A>C	GRCh37
NC_000004.10:g.74504111A>C	NCBI36
NG_009291.1:g.20276A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1676A>C MANE Select	ENSP00000295897.4:p.His559Pro
ENST00000295897.8:c.1676A>C	ENSP00000295897.4:p.His559Pro
ENST00000401494.7:c.1331A>C	ENSP00000384695.3:p.His444Pro
ENST00000415165.6:c.1100A>C	ENSP00000401820.2:p.His367Pro
ENST00000476441.6:c.*955A>C	ENSP00000423727.1:n.*955A>C
ENST00000486939.1:n.330A>C
ENST00000503124.5:c.1226A>C	ENSP00000421027.1:p.His409Pro
ENST00000505649.5:n.1223A>C
ENST00000508932.5:n.175+75A>C
ENST00000509063.5:c.1676A>C	ENSP00000422784.1:p.His559Pro
ENST00000511370.1:c.1209A>C
ENST00000621085.4:c.1037A>C	ENSP00000483421.1:p.His346Pro
ENST00000621628.4:c.1037A>C	ENSP00000480485.1:p.His346Pro
NM_000477.5:c.1676A>C	NP_000468.1:p.His559Pro
NM_000477.6:c.1676A>C	NP_000468.1:p.His559Pro
NM_000477.7:c.1676A>C MANE Select	NP_000468.1:p.His559Pro