Canonical Allele Identifier: CA1468152537

Gene: ALB

Linked Data

• dbSNP Id: rs1718803847

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73409113A>G , CM000666.2:g.73409113A>G	GRCh38
NC_000004.11:g.74274830A>G , CM000666.1:g.74274830A>G	GRCh37
NC_000004.10:g.74493694A>G	NCBI36
NG_009291.1:g.9859A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.483-242A>G MANE Select	ENSP00000295897.4:n.483-242A>G
ENST00000295897.8:c.483-242A>G	ENSP00000295897.4:n.483-242A>G
ENST00000401494.7:c.138-242A>G	ENSP00000384695.3:n.138-242A>G
ENST00000415165.6:c.138-2883A>G	ENSP00000401820.2:n.138-2883A>G
ENST00000441319.5:c.489-242A>G	ENSP00000392541.1:n.489-242A>G
ENST00000476441.6:c.80-242A>G	ENSP00000423727.1:n.80-242A>G
ENST00000503124.5:c.33-242A>G	ENSP00000421027.1:n.33-242A>G
ENST00000505649.5:n.169-242A>G
ENST00000509063.5:c.483-242A>G	ENSP00000422784.1:n.483-242A>G
ENST00000514786.1:n.452-242A>G
ENST00000621085.4:c.483-242A>G	ENSP00000483421.1:n.483-242A>G
ENST00000621628.4:c.486+37A>G	ENSP00000480485.1:n.486+37A>G
NM_000477.5:c.483-242A>G	NP_000468.1:n.483-242A>G
NM_000477.6:c.483-242A>G	NP_000468.1:n.483-242A>G
NM_000477.7:c.483-242A>G MANE Select	NP_000468.1:n.483-242A>G