Canonical Allele Identifier: CA2670966546

Gene: ALB

Linked Data

• gnomAD v4: 4-73419440-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73419440C>T , CM000666.2:g.73419440C>T	GRCh38
NC_000004.11:g.74285157C>T , CM000666.1:g.74285157C>T	GRCh37
NC_000004.10:g.74504021C>T	NCBI36
NG_009291.1:g.20186C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1653-67C>T MANE Select	ENSP00000295897.4:n.1653-67C>T
ENST00000295897.8:c.1653-67C>T	ENSP00000295897.4:n.1653-67C>T
ENST00000401494.7:c.1308-67C>T	ENSP00000384695.3:n.1308-67C>T
ENST00000415165.6:c.1077-67C>T	ENSP00000401820.2:n.1077-67C>T
ENST00000476441.6:c.*932-67C>T	ENSP00000423727.1:n.*932-67C>T
ENST00000486939.1:n.307-67C>T
ENST00000503124.5:c.1203-67C>T	ENSP00000421027.1:n.1203-67C>T
ENST00000505649.5:n.1200-67C>T
ENST00000508932.5:n.160C>T
ENST00000509063.5:c.1653-67C>T	ENSP00000422784.1:n.1653-67C>T
ENST00000511370.1:c.1186-67C>T
ENST00000621085.4:c.1014-67C>T	ENSP00000483421.1:n.1014-67C>T
ENST00000621628.4:c.1014-67C>T	ENSP00000480485.1:n.1014-67C>T
NM_000477.5:c.1653-67C>T	NP_000468.1:n.1653-67C>T
NM_000477.6:c.1653-67C>T	NP_000468.1:n.1653-67C>T
NM_000477.7:c.1653-67C>T MANE Select	NP_000468.1:n.1653-67C>T