Canonical Allele Identifier: CA2959547

Gene: ALB

Linked Data

• dbSNP Id: rs770576681
• ExAC: 4:74280780 C / A
• gnomAD v2: 4-74280780-C-A
• gnomAD v4: 4-73415063-C-A
• MyVariant Identifiers: chr4:g.74280780C>A (hg19) ; chr4:g.73415063C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415063C>A , CM000666.2:g.73415063C>A	GRCh38
NC_000004.11:g.74280780C>A , CM000666.1:g.74280780C>A	GRCh37
NC_000004.10:g.74499644C>A	NCBI36
NG_009291.1:g.15809C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1087C>A MANE Select	ENSP00000295897.4:p.Pro363Thr
ENST00000295897.8:c.1087C>A	ENSP00000295897.4:p.Pro363Thr
ENST00000401494.7:c.742C>A	ENSP00000384695.3:p.Pro248Thr
ENST00000415165.6:c.511C>A	ENSP00000401820.2:p.Pro171Thr
ENST00000476441.6:c.*366C>A	ENSP00000423727.1:n.*366C>A
ENST00000484992.1:n.407C>A
ENST00000503124.5:c.637C>A	ENSP00000421027.1:p.Pro213Thr
ENST00000504043.1:n.90C>A
ENST00000505649.5:n.773C>A
ENST00000509063.5:c.1087C>A	ENSP00000422784.1:p.Pro363Thr
ENST00000511370.1:c.620C>A
ENST00000621085.4:c.491-43C>A	ENSP00000483421.1:n.491-43C>A
ENST00000621628.4:c.487-39C>A	ENSP00000480485.1:n.487-39C>A
NM_000477.5:c.1087C>A	NP_000468.1:p.Pro363Thr
NM_000477.6:c.1087C>A	NP_000468.1:p.Pro363Thr
NM_000477.7:c.1087C>A MANE Select	NP_000468.1:p.Pro363Thr